rs750529207

Orientation

plus

Stabilized

plus

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

Make rs750529207(A;A)

Make rs750529207(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

149028147

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs750529207
dbSNP (classic)	rs750529207
ClinGen	rs750529207
ebi	rs750529207
HLI	rs750529207
Exac	rs750529207
Gnomad	rs750529207
Varsome	rs750529207
LitVar	rs750529207
Map	rs750529207
PheGenI	rs750529207
Biobank	rs750529207
1000 genomes	rs750529207
hgdp	rs750529207
ensembl	rs750529207
geneview	rs750529207
scholar	rs750529207
google	rs750529207
pharmgkb	rs750529207
gwascentral	rs750529207
openSNP	rs750529207
23andMe	rs750529207
SNPshot	rs750529207
SNPdbe	rs750529207
MSV3d	rs750529207
GWAS Ctlg	rs750529207

Max Magnitude

0

ClinVar
Risk	rs750529207(A;A)
Alt	rs750529207(A;A)
Reference	Rs750529207(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SH3TC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.148407710G>A
CLNSRC
CLNACC	RCV000484690.1,