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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
170219011
T
C
5_prime_UTR_variant
MODIFIER
LRP2
c.-102A>G
chr2
170218847
C
G
synonymous_variant
LOW
LRP2
c.63G>C
chr2
170218816
T
C
intron_variant
MODIFIER
LRP2
c.79+15A>G
chr2
170151227
TAAAAA
T
splice_region_variant&intron_variant
LOW
LRP2
c.428-12_428-8delTTTTT
chr2
170145426
G
A
intron_variant
MODIFIER
LRP2
c.1042+110C>T
chr2
170139346
C
T
intron_variant
MODIFIER
LRP2
c.1171+37G>A
chr2
170134191
G
C
intron_variant
MODIFIER
LRP2
c.1772+64C>G
chr2
170129636
A
G
intron_variant
MODIFIER
LRP2
c.1976-59T>C
chr2
170129528
G
A
synonymous_variant
LOW
LRP2
c.2025C>T
chr2
170115588
T
C
synonymous_variant
LOW
LRP2
c.2460A>G
chr2
170103351
G
T
synonymous_variant
LOW
LRP2
c.3054C>A
chr2
170103336
T
C
synonymous_variant
LOW
LRP2
c.3069A>G
chr2
170099899
G
A
intron_variant
MODIFIER
LRP2
c.3550+14C>T
chr2
170099895
A
C
intron_variant
MODIFIER
LRP2
c.3550+18T>G
chr2
170099473
T
C
synonymous_variant
LOW
LRP2
c.3660A>G
chr2
170099446
T
G
intron_variant
MODIFIER
LRP2
c.3667+20A>C
chr2
170096018
G
A
intron_variant
MODIFIER
LRP2
c.4294+19C>T
chr2
170092395
A
G
synonymous_variant
LOW
LRP2
c.4875T>C
chr2
170089851
G
A
intron_variant
MODIFIER
LRP2
c.5098+70C>T
chr2
170089824
T
C
intron_variant
MODIFIER
LRP2
c.5098+97A>G