rs876661203

Orientation

minus

Stabilized

minus

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

Make rs876661203(A;A)

Make rs876661203(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

5973466

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs876661203
dbSNP (classic)	rs876661203
ClinGen	rs876661203
ebi	rs876661203
HLI	rs876661203
Exac	rs876661203
Gnomad	rs876661203
Varsome	rs876661203
LitVar	rs876661203
Map	rs876661203
PheGenI	rs876661203
Biobank	rs876661203
1000 genomes	rs876661203
hgdp	rs876661203
ensembl	rs876661203
geneview	rs876661203
scholar	rs876661203
google	rs876661203
pharmgkb	rs876661203
gwascentral	rs876661203
openSNP	rs876661203
23andMe	rs876661203
SNPshot	rs876661203
SNPdbe	rs876661203
MSV3d	rs876661203
GWAS Ctlg	rs876661203

Max Magnitude

0

ClinVar
Risk	rs876661203(A;A)
Alt	rs876661203(A;A)
Reference	Rs876661203(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PMS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.6013097C>T
CLNSRC
CLNACC	RCV000217259.1,