rs387906932

Orientation

plus

Stabilized

plus

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

Make rs387906932(C;T)

Make rs387906932(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

50721182

Gene

SHANK3

is a	snp
is	mentioned by
dbSNP	rs387906932
dbSNP (classic)	rs387906932
ClinGen	rs387906932
ebi	rs387906932
HLI	rs387906932
Exac	rs387906932
Gnomad	rs387906932
Varsome	rs387906932
LitVar	rs387906932
Map	rs387906932
PheGenI	rs387906932
Biobank	rs387906932
1000 genomes	rs387906932
hgdp	rs387906932
ensembl	rs387906932
geneview	rs387906932
scholar	rs387906932
google	rs387906932
pharmgkb	rs387906932
gwascentral	rs387906932
openSNP	rs387906932
23andMe	rs387906932
SNPshot	rs387906932
SNPdbe	rs387906932
MSV3d	rs387906932
GWAS Ctlg	rs387906932

Max Magnitude

0

ClinVar
Risk	rs387906932(T;T)
Alt	rs387906932(T;T)
Reference	Rs387906932(C;C)
Significance	Pathogenic
Disease	Schizophrenia 15
Variation	info
Gene	SHANK3
CLNDBN	Schizophrenia 15
Reversed	0
HGVS	NC_000022.10:g.51159610C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023519.3,