rs749850181

Orientation

plus

Stabilized

plus

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

Make rs749850181(A;A)

Make rs749850181(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

149028348

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs749850181
dbSNP (classic)	rs749850181
ClinGen	rs749850181
ebi	rs749850181
HLI	rs749850181
Exac	rs749850181
Gnomad	rs749850181
Varsome	rs749850181
LitVar	rs749850181
Map	rs749850181
PheGenI	rs749850181
Biobank	rs749850181
1000 genomes	rs749850181
hgdp	rs749850181
ensembl	rs749850181
geneview	rs749850181
scholar	rs749850181
google	rs749850181
pharmgkb	rs749850181
gwascentral	rs749850181
openSNP	rs749850181
23andMe	rs749850181
SNPshot	rs749850181
SNPdbe	rs749850181
MSV3d	rs749850181
GWAS Ctlg	rs749850181

Max Magnitude

0

ClinVar
Risk	rs749850181(A;A)
Alt	rs749850181(A;A)
Reference	Rs749850181(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SH3TC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.148407911C>A
CLNSRC
CLNACC	RCV000214436.1,