rs876660075

Orientation

minus

Stabilized

minus

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

Make rs876660075(-;-)

Make rs876660075(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

5991972

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs876660075
dbSNP (classic)	rs876660075
ClinGen	rs876660075
ebi	rs876660075
HLI	rs876660075
Exac	rs876660075
Gnomad	rs876660075
Varsome	rs876660075
LitVar	rs876660075
Map	rs876660075
PheGenI	rs876660075
Biobank	rs876660075
1000 genomes	rs876660075
hgdp	rs876660075
ensembl	rs876660075
geneview	rs876660075
scholar	rs876660075
google	rs876660075
pharmgkb	rs876660075
gwascentral	rs876660075
openSNP	rs876660075
23andMe	rs876660075
SNPshot	rs876660075
SNPdbe	rs876660075
MSV3d	rs876660075
GWAS Ctlg	rs876660075

Max Magnitude

0

ClinVar
Risk	rs876660075(-;-)
Alt	rs876660075(-;-)
Reference	Rs876660075(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000007.13:g.6031603delC
CLNSRC
CLNACC	RCV000216559.1,