rs876661113

Orientation

minus

Stabilized

minus

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

Make rs876661113(G;T)

Make rs876661113(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

5977587

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs876661113
dbSNP (classic)	rs876661113
ClinGen	rs876661113
ebi	rs876661113
HLI	rs876661113
Exac	rs876661113
Gnomad	rs876661113
Varsome	rs876661113
LitVar	rs876661113
Map	rs876661113
PheGenI	rs876661113
Biobank	rs876661113
1000 genomes	rs876661113
hgdp	rs876661113
ensembl	rs876661113
geneview	rs876661113
scholar	rs876661113
google	rs876661113
pharmgkb	rs876661113
gwascentral	rs876661113
openSNP	rs876661113
23andMe	rs876661113
SNPshot	rs876661113
SNPdbe	rs876661113
MSV3d	rs876661113
GWAS Ctlg	rs876661113

Max Magnitude

0

ClinVar
Risk	rs876661113(C;C) rs876661113(T;T)
Alt	rs876661113(C;C) rs876661113(T;T)
Reference	Rs876661113(G;G)
Significance	Pathogenic
Disease	not provided Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	not provided Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6017218C>A; NC_000007.13:g.6017218C>G
CLNSRC
CLNACC	RCV000219334.1, RCV000228982.2, RCV000234016.1,