rs387907337

Orientation

minus

Stabilized

minus

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

Make rs387907337(C;T)

Make rs387907337(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

111911667

Gene	CRYAB, HSPB2, HSPB2-C11orf52

is a	snp
is	mentioned by
dbSNP	rs387907337
dbSNP (classic)	rs387907337
ClinGen	rs387907337
ebi	rs387907337
HLI	rs387907337
Exac	rs387907337
Gnomad	rs387907337
Varsome	rs387907337
LitVar	rs387907337
Map	rs387907337
PheGenI	rs387907337
Biobank	rs387907337
1000 genomes	rs387907337
hgdp	rs387907337
ensembl	rs387907337
geneview	rs387907337
scholar	rs387907337
google	rs387907337
pharmgkb	rs387907337
gwascentral	rs387907337
openSNP	rs387907337
23andMe	rs387907337
SNPshot	rs387907337
SNPdbe	rs387907337
MSV3d	rs387907337
GWAS Ctlg	rs387907337

Max Magnitude

0

ClinVar
Risk	rs387907337(T;T)
Alt	rs387907337(T;T)
Reference	Rs387907337(C;C)
Significance	Pathogenic
Disease	Cataract 16
Variation	info
Gene	HSPB2-C11orf52 HSPB2 CRYAB
CLNDBN	Cataract 16, multiple types
Reversed	1
HGVS	NC_000011.9:g.111782391G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000034841.30,