rs397517237

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GTT;GTT)	0	common in clinvar
(TGT;TGT)	0	common in clinvar

Make rs397517237(-;-)

Make rs397517237(-;GTT)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

74112025

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs397517237
dbSNP (classic)	rs397517237
ClinGen	rs397517237
ebi	rs397517237
HLI	rs397517237
Exac	rs397517237
Gnomad	rs397517237
Varsome	rs397517237
LitVar	rs397517237
Map	rs397517237
PheGenI	rs397517237
Biobank	rs397517237
1000 genomes	rs397517237
hgdp	rs397517237
ensembl	rs397517237
geneview	rs397517237
scholar	rs397517237
google	rs397517237
pharmgkb	rs397517237
gwascentral	rs397517237
openSNP	rs397517237
23andMe	rs397517237
SNPshot	rs397517237
SNPdbe	rs397517237
MSV3d	rs397517237
GWAS Ctlg	rs397517237

Max Magnitude

0

ClinVar
Risk	rs397517237(-;-) Rs397517237(TGT;TGT)
Alt	rs397517237(-;-) Rs397517237(TGT;TGT)
Reference	Rs397517237(GTT;GTT)
Significance	Probable-Pathogenic
Disease	not specified Dilated cardiomyopathy Dilated cardiomyopathy 1W
Variation	info
Gene	VCL
CLNDBN	not specified Dilated cardiomyopathy Dilated cardiomyopathy 1W
Reversed	0
HGVS	NC_000010.10:g.75871783_75871785delGTT
CLNSRC
CLNACC	RCV000038819.5, RCV000171847.1, RCV000225812.2,