rs200728983

Orientation

plus

Stabilized

plus

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

Make rs200728983(C;T)

Make rs200728983(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

149007044

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs200728983
dbSNP (classic)	rs200728983
ClinGen	rs200728983
ebi	rs200728983
HLI	rs200728983
Exac	rs200728983
Gnomad	rs200728983
Varsome	rs200728983
LitVar	rs200728983
Map	rs200728983
PheGenI	rs200728983
Biobank	rs200728983
1000 genomes	rs200728983
hgdp	rs200728983
ensembl	rs200728983
geneview	rs200728983
scholar	rs200728983
google	rs200728983
pharmgkb	rs200728983
gwascentral	rs200728983
openSNP	rs200728983
23andMe	rs200728983
SNPshot	rs200728983
SNPdbe	rs200728983
MSV3d	rs200728983
GWAS Ctlg	rs200728983

Max Magnitude

0

ClinVar
Risk	rs200728983(A;A) rs200728983(T;T)
Alt	rs200728983(A;A) rs200728983(T;T)
Reference	Rs200728983(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SH3TC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.148386607C>A
CLNSRC
CLNACC	RCV000236255.1,