rs863224167

Orientation

minus

Stabilized

minus

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

Make rs863224167(A;G)

Make rs863224167(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

107212111

Gene

PDSS2

is a	snp
is	mentioned by
dbSNP	rs863224167
dbSNP (classic)	rs863224167
ClinGen	rs863224167
ebi	rs863224167
HLI	rs863224167
Exac	rs863224167
Gnomad	rs863224167
Varsome	rs863224167
LitVar	rs863224167
Map	rs863224167
PheGenI	rs863224167
Biobank	rs863224167
1000 genomes	rs863224167
hgdp	rs863224167
ensembl	rs863224167
geneview	rs863224167
scholar	rs863224167
google	rs863224167
pharmgkb	rs863224167
gwascentral	rs863224167
openSNP	rs863224167
23andMe	rs863224167
SNPshot	rs863224167
SNPdbe	rs863224167
MSV3d	rs863224167
GWAS Ctlg	rs863224167

Max Magnitude

0

ClinVar
Risk	rs863224167(G;G)
Alt	rs863224167(G;G)
Reference	Rs863224167(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PDSS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.107533315T>C
CLNSRC
CLNACC	RCV000196261.1,