rs878854035

Orientation

minus

Stabilized

minus

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

Make rs878854035(-;C)

Make rs878854035(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

5987264

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs878854035
dbSNP (classic)	rs878854035
ClinGen	rs878854035
ebi	rs878854035
HLI	rs878854035
Exac	rs878854035
Gnomad	rs878854035
Varsome	rs878854035
LitVar	rs878854035
Map	rs878854035
PheGenI	rs878854035
Biobank	rs878854035
1000 genomes	rs878854035
hgdp	rs878854035
ensembl	rs878854035
geneview	rs878854035
scholar	rs878854035
google	rs878854035
pharmgkb	rs878854035
gwascentral	rs878854035
openSNP	rs878854035
23andMe	rs878854035
SNPshot	rs878854035
SNPdbe	rs878854035
MSV3d	rs878854035
GWAS Ctlg	rs878854035

Max Magnitude

0

ClinVar
Risk	rs878854035(C;C)
Alt	rs878854035(C;C)
Reference	Rs878854035(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6026896dupG
CLNSRC
CLNACC	RCV000230207.1,