rs879254317

Orientation

minus

Stabilized

minus

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

Make rs879254317(G;T)

Make rs879254317(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

149027244

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs879254317
dbSNP (classic)	rs879254317
ClinGen	rs879254317
ebi	rs879254317
HLI	rs879254317
Exac	rs879254317
Gnomad	rs879254317
Varsome	rs879254317
LitVar	rs879254317
Map	rs879254317
PheGenI	rs879254317
Biobank	rs879254317
1000 genomes	rs879254317
hgdp	rs879254317
ensembl	rs879254317
geneview	rs879254317
scholar	rs879254317
google	rs879254317
pharmgkb	rs879254317
gwascentral	rs879254317
openSNP	rs879254317
23andMe	rs879254317
SNPshot	rs879254317
SNPdbe	rs879254317
MSV3d	rs879254317
GWAS Ctlg	rs879254317

Max Magnitude

0

ClinVar
Risk	rs879254317(T;T)
Alt	rs879254317(T;T)
Reference	Rs879254317(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SH3TC2
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.148406807C>A
CLNSRC
CLNACC	RCV000235715.1,