rs121917776

Orientation

plus

Stabilized

plus

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

Make rs121917776(C;T)

Make rs121917776(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

74112086

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs121917776
dbSNP (classic)	rs121917776
ClinGen	rs121917776
ebi	rs121917776
HLI	rs121917776
Exac	rs121917776
Gnomad	rs121917776
Varsome	rs121917776
LitVar	rs121917776
Map	rs121917776
PheGenI	rs121917776
Biobank	rs121917776
1000 genomes	rs121917776
hgdp	rs121917776
ensembl	rs121917776
geneview	rs121917776
scholar	rs121917776
google	rs121917776
pharmgkb	rs121917776
gwascentral	rs121917776
openSNP	rs121917776
23andMe	rs121917776
SNPshot	rs121917776
SNPdbe	rs121917776
MSV3d	rs121917776
GWAS Ctlg	rs121917776

Max Magnitude

0

OMIM	193065
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121917776(T;T)
Alt	rs121917776(T;T)
Reference	Rs121917776(C;C)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 1W Familial hypertrophic cardiomyopathy 15
Variation	info
Gene	VCL
CLNDBN	Dilated cardiomyopathy 1W Familial hypertrophic cardiomyopathy 15
Reversed	0
HGVS	NC_000010.10:g.75871844C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012980.16, RCV000012981.22,