rs863224166

Orientation

minus

Stabilized

minus

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

Make rs863224166(A;G)

Make rs863224166(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

107210572

Gene

PDSS2

is a	snp
is	mentioned by
dbSNP	rs863224166
dbSNP (classic)	rs863224166
ClinGen	rs863224166
ebi	rs863224166
HLI	rs863224166
Exac	rs863224166
Gnomad	rs863224166
Varsome	rs863224166
LitVar	rs863224166
Map	rs863224166
PheGenI	rs863224166
Biobank	rs863224166
1000 genomes	rs863224166
hgdp	rs863224166
ensembl	rs863224166
geneview	rs863224166
scholar	rs863224166
google	rs863224166
pharmgkb	rs863224166
gwascentral	rs863224166
openSNP	rs863224166
23andMe	rs863224166
SNPshot	rs863224166
SNPdbe	rs863224166
MSV3d	rs863224166
GWAS Ctlg	rs863224166

Max Magnitude

0

ClinVar
Risk	rs863224166(G;G)
Alt	rs863224166(G;G)
Reference	Rs863224166(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PDSS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.107531776T>C
CLNSRC
CLNACC	RCV000199826.2,