rs387907336

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs387907336(A;A)

Make rs387907336(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

111908874

Gene

CRYAB

is a	snp
is	mentioned by
dbSNP	rs387907336
dbSNP (classic)	rs387907336
ClinGen	rs387907336
ebi	rs387907336
HLI	rs387907336
Exac	rs387907336
Gnomad	rs387907336
Varsome	rs387907336
LitVar	rs387907336
Map	rs387907336
PheGenI	rs387907336
Biobank	rs387907336
1000 genomes	rs387907336
hgdp	rs387907336
ensembl	rs387907336
geneview	rs387907336
scholar	rs387907336
google	rs387907336
pharmgkb	rs387907336
gwascentral	rs387907336
openSNP	rs387907336
23andMe	rs387907336
SNPshot	rs387907336
SNPdbe	rs387907336
MSV3d	rs387907336
GWAS Ctlg	rs387907336

Max Magnitude

0

ClinVar
Risk	rs387907336(A;A)
Alt	rs387907336(A;A)
Reference	Rs387907336(G;G)
Significance	Pathogenic
Disease	Cataract 16
Variation	info
Gene	CRYAB
CLNDBN	Cataract 16, multiple types
Reversed	1
HGVS	NC_000011.9:g.111779598C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000034840.30,