rs863225121

Orientation

plus

Stabilized

plus

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

Make rs863225121(G;T)

Make rs863225121(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

74094449

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs863225121
dbSNP (classic)	rs863225121
ClinGen	rs863225121
ebi	rs863225121
HLI	rs863225121
Exac	rs863225121
Gnomad	rs863225121
Varsome	rs863225121
LitVar	rs863225121
Map	rs863225121
PheGenI	rs863225121
Biobank	rs863225121
1000 genomes	rs863225121
hgdp	rs863225121
ensembl	rs863225121
geneview	rs863225121
scholar	rs863225121
google	rs863225121
pharmgkb	rs863225121
gwascentral	rs863225121
openSNP	rs863225121
23andMe	rs863225121
SNPshot	rs863225121
SNPdbe	rs863225121
MSV3d	rs863225121
GWAS Ctlg	rs863225121

Max Magnitude

0

ClinVar
Risk	rs863225121(T;T)
Alt	rs863225121(T;T)
Reference	Rs863225121(G;G)
Significance	Probable-Pathogenic
Disease	Familial hypertrophic cardiomyopathy 15
Variation	info
Gene	VCL
CLNDBN	Familial hypertrophic cardiomyopathy 15
Reversed	0
HGVS	NC_000010.10:g.75854207G>T
CLNSRC
CLNACC	RCV000201438.1,