rs281865141

Orientation

minus

Stabilized

minus

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

Make rs281865141(-;-)

Make rs281865141(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

111911665

Gene	CRYAB, HSPB2, HSPB2-C11orf52

is a	snp
is	mentioned by
dbSNP	rs281865141
dbSNP (classic)	rs281865141
ClinGen	rs281865141
ebi	rs281865141
HLI	rs281865141
Exac	rs281865141
Gnomad	rs281865141
Varsome	rs281865141
LitVar	rs281865141
Map	rs281865141
PheGenI	rs281865141
Biobank	rs281865141
1000 genomes	rs281865141
hgdp	rs281865141
ensembl	rs281865141
geneview	rs281865141
scholar	rs281865141
google	rs281865141
pharmgkb	rs281865141
gwascentral	rs281865141
openSNP	rs281865141
23andMe	rs281865141
SNPshot	rs281865141
SNPdbe	rs281865141
MSV3d	rs281865141
GWAS Ctlg	rs281865141

Max Magnitude

0

ClinVar
Risk	rs281865141(-;-)
Alt	rs281865141(-;-)
Reference	Rs281865141(C;C)
Significance	Pathogenic
Disease	Alpha-B crystallinopathy
Variation	info
Gene	HSPB2-C11orf52 HSPB2 CRYAB
CLNDBN	Alpha-B crystallinopathy
Reversed	1
HGVS	NC_000011.9:g.111782389delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043523.28,