rs71579353

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs71579353(A;A)

Make rs71579353(A;C)

Reference

GRCh38 38.1/141

Chromosome

10

Position

74082499

Gene	LOC107984244, VCL

is a	snp
is	mentioned by
dbSNP	rs71579353
dbSNP (classic)	rs71579353
ClinGen	rs71579353
ebi	rs71579353
HLI	rs71579353
Exac	rs71579353
Gnomad	rs71579353
Varsome	rs71579353
LitVar	rs71579353
Map	rs71579353
PheGenI	rs71579353
Biobank	rs71579353
1000 genomes	rs71579353
hgdp	rs71579353
ensembl	rs71579353
geneview	rs71579353
scholar	rs71579353
google	rs71579353
pharmgkb	rs71579353
gwascentral	rs71579353
openSNP	rs71579353
23andMe	rs71579353
SNPshot	rs71579353
SNPdbe	rs71579353
MSV3d	rs71579353
GWAS Ctlg	rs71579353

Max Magnitude

0

OMIM	193065
Desc
Variant	0003
Related	also

ClinVar
Risk	rs71579353(A;A)
Alt	rs71579353(A;A)
Reference	Rs71579353(C;C)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 15
Variation	info
Gene	VCL
CLNDBN	Familial hypertrophic cardiomyopathy 15
Reversed	0
HGVS	NC_000010.10:g.75842257C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012982.16,