rs772823083

Orientation

plus

Stabilized

plus

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

Make rs772823083(C;T)

Make rs772823083(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

149004910

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs772823083
dbSNP (classic)	rs772823083
ClinGen	rs772823083
ebi	rs772823083
HLI	rs772823083
Exac	rs772823083
Gnomad	rs772823083
Varsome	rs772823083
LitVar	rs772823083
Map	rs772823083
PheGenI	rs772823083
Biobank	rs772823083
1000 genomes	rs772823083
hgdp	rs772823083
ensembl	rs772823083
geneview	rs772823083
scholar	rs772823083
google	rs772823083
pharmgkb	rs772823083
gwascentral	rs772823083
openSNP	rs772823083
23andMe	rs772823083
SNPshot	rs772823083
SNPdbe	rs772823083
MSV3d	rs772823083
GWAS Ctlg	rs772823083

Max Magnitude

0

ClinVar
Risk	rs772823083(T;T)
Alt	rs772823083(T;T)
Reference	Rs772823083(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SH3TC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.148384473C>T
CLNSRC
CLNACC	RCV000489941.1,