rs786202098

Orientation

minus

Stabilized

minus

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

Make rs786202098(A;G)

Make rs786202098(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

6002638

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs786202098
dbSNP (classic)	rs786202098
ClinGen	rs786202098
ebi	rs786202098
HLI	rs786202098
Exac	rs786202098
Gnomad	rs786202098
Varsome	rs786202098
LitVar	rs786202098
Map	rs786202098
PheGenI	rs786202098
Biobank	rs786202098
1000 genomes	rs786202098
hgdp	rs786202098
ensembl	rs786202098
geneview	rs786202098
scholar	rs786202098
google	rs786202098
pharmgkb	rs786202098
gwascentral	rs786202098
openSNP	rs786202098
23andMe	rs786202098
SNPshot	rs786202098
SNPdbe	rs786202098
MSV3d	rs786202098
GWAS Ctlg	rs786202098

Max Magnitude

0

ClinVar
Risk	rs786202098(G;G)
Alt	rs786202098(G;G)
Reference	Rs786202098(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000007.13:g.6042269T>C
CLNSRC
CLNACC	RCV000164744.1,