rs876658862

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	6	Lynch syndrome

Make rs876658862(C;T)

Make rs876658862(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

5987567

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs876658862
dbSNP (classic)	rs876658862
ClinGen	rs876658862
ebi	rs876658862
HLI	rs876658862
Exac	rs876658862
Gnomad	rs876658862
Varsome	rs876658862
LitVar	rs876658862
Map	rs876658862
PheGenI	rs876658862
Biobank	rs876658862
1000 genomes	rs876658862
hgdp	rs876658862
ensembl	rs876658862
geneview	rs876658862
scholar	rs876658862
google	rs876658862
pharmgkb	rs876658862
gwascentral	rs876658862
openSNP	rs876658862
23andMe	rs876658862
SNPshot	rs876658862
SNPdbe	rs876658862
MSV3d	rs876658862
GWAS Ctlg	rs876658862

Max Magnitude

6

ClinVar
Risk	rs876658862(T;T)
Alt	rs876658862(T;T)
Reference	Rs876658862(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000007.13:g.6027198G>A
CLNSRC
CLNACC	RCV000220993.1,