rs767325003

Orientation

plus

Stabilized

plus

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

Make rs767325003(A;A)

Make rs767325003(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

74112087

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs767325003
dbSNP (classic)	rs767325003
ClinGen	rs767325003
ebi	rs767325003
HLI	rs767325003
Exac	rs767325003
Gnomad	rs767325003
Varsome	rs767325003
LitVar	rs767325003
Map	rs767325003
PheGenI	rs767325003
Biobank	rs767325003
1000 genomes	rs767325003
hgdp	rs767325003
ensembl	rs767325003
geneview	rs767325003
scholar	rs767325003
google	rs767325003
pharmgkb	rs767325003
gwascentral	rs767325003
openSNP	rs767325003
23andMe	rs767325003
SNPshot	rs767325003
SNPdbe	rs767325003
MSV3d	rs767325003
GWAS Ctlg	rs767325003

Max Magnitude

0

ClinVar
Risk	rs767325003(A;A) rs767325003(T;T)
Alt	rs767325003(A;A) rs767325003(T;T)
Reference	Rs767325003(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	VCL
CLNDBN	not specified
Reversed	0
HGVS	NC_000010.10:g.75871845G>A
CLNSRC
CLNACC	RCV000171177.2,