rs398123688

Orientation

plus

Stabilized

plus

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

Make rs398123688(G;T)

Make rs398123688(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

11449338

Gene

PRKCSH

is a	snp
is	mentioned by
dbSNP	rs398123688
dbSNP (classic)	rs398123688
ClinGen	rs398123688
ebi	rs398123688
HLI	rs398123688
Exac	rs398123688
Gnomad	rs398123688
Varsome	rs398123688
LitVar	rs398123688
Map	rs398123688
PheGenI	rs398123688
Biobank	rs398123688
1000 genomes	rs398123688
hgdp	rs398123688
ensembl	rs398123688
geneview	rs398123688
scholar	rs398123688
google	rs398123688
pharmgkb	rs398123688
gwascentral	rs398123688
openSNP	rs398123688
23andMe	rs398123688
SNPshot	rs398123688
SNPdbe	rs398123688
MSV3d	rs398123688
GWAS Ctlg	rs398123688

Max Magnitude

0

ClinVar
Risk	rs398123688(T;T)
Alt	rs398123688(T;T)
Reference	Rs398123688(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PRKCSH
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.11560153G>T
CLNSRC	ClinVar Emory University
CLNACC	RCV000080024.4,