rs786201062

Orientation

minus

Stabilized

minus

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

Make rs786201062(-;-)

Make rs786201062(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

5982842

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs786201062
dbSNP (classic)	rs786201062
ClinGen	rs786201062
ebi	rs786201062
HLI	rs786201062
Exac	rs786201062
Gnomad	rs786201062
Varsome	rs786201062
LitVar	rs786201062
Map	rs786201062
PheGenI	rs786201062
Biobank	rs786201062
1000 genomes	rs786201062
hgdp	rs786201062
ensembl	rs786201062
geneview	rs786201062
scholar	rs786201062
google	rs786201062
pharmgkb	rs786201062
gwascentral	rs786201062
openSNP	rs786201062
23andMe	rs786201062
SNPshot	rs786201062
SNPdbe	rs786201062
MSV3d	rs786201062
GWAS Ctlg	rs786201062

Max Magnitude

0

ClinVar
Risk	rs786201062(-;-)
Alt	rs786201062(-;-)
Reference	Rs786201062(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000007.13:g.6022473delT
CLNSRC
CLNACC	RCV000162471.1, RCV000482434.1,