rs786201039

Orientation

minus

Stabilized

minus

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

Make rs786201039(G;T)

Make rs786201039(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

5973482

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs786201039
dbSNP (classic)	rs786201039
ClinGen	rs786201039
ebi	rs786201039
HLI	rs786201039
Exac	rs786201039
Gnomad	rs786201039
Varsome	rs786201039
LitVar	rs786201039
Map	rs786201039
PheGenI	rs786201039
Biobank	rs786201039
1000 genomes	rs786201039
hgdp	rs786201039
ensembl	rs786201039
geneview	rs786201039
scholar	rs786201039
google	rs786201039
pharmgkb	rs786201039
gwascentral	rs786201039
openSNP	rs786201039
23andMe	rs786201039
SNPshot	rs786201039
SNPdbe	rs786201039
MSV3d	rs786201039
GWAS Ctlg	rs786201039

Max Magnitude

0

ClinVar
Risk	rs786201039(A;A) rs786201039(T;T)
Alt	rs786201039(A;A) rs786201039(T;T)
Reference	Rs786201039(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000007.13:g.6013113C>A
CLNSRC
CLNACC	RCV000162416.1,