rs121917775

Orientation

plus

Stabilized

plus

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

Make rs121917775(A;A)

Make rs121917775(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

17229873

Gene	VIM, VIM-AS1

is a	snp
is	mentioned by
dbSNP	rs121917775
dbSNP (classic)	rs121917775
ClinGen	rs121917775
ebi	rs121917775
HLI	rs121917775
Exac	rs121917775
Gnomad	rs121917775
Varsome	rs121917775
LitVar	rs121917775
Map	rs121917775
PheGenI	rs121917775
Biobank	rs121917775
1000 genomes	rs121917775
hgdp	rs121917775
ensembl	rs121917775
geneview	rs121917775
scholar	rs121917775
google	rs121917775
pharmgkb	rs121917775
gwascentral	rs121917775
openSNP	rs121917775
23andMe	rs121917775
SNPshot	rs121917775
SNPdbe	rs121917775
MSV3d	rs121917775
GWAS Ctlg	rs121917775

Max Magnitude

0

OMIM	193060
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121917775(A;A)
Alt	rs121917775(A;A)
Reference	Rs121917775(G;G)
Significance	Pathogenic
Disease	Cataract 30 not provided
Variation	info
Gene	VIM-AS1 VIM
CLNDBN	Cataract 30, multiple types not provided
Reversed	0
HGVS	NC_000010.10:g.17271872G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012983.25, RCV000056967.1,