rs267608156

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;T)	6	Lynch syndrome, pathogenic mutation

Make rs267608156(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

5989867

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs267608156
dbSNP (classic)	rs267608156
ClinGen	rs267608156
ebi	rs267608156
HLI	rs267608156
Exac	rs267608156
Gnomad	rs267608156
Varsome	rs267608156
LitVar	rs267608156
Map	rs267608156
PheGenI	rs267608156
Biobank	rs267608156
1000 genomes	rs267608156
hgdp	rs267608156
ensembl	rs267608156
geneview	rs267608156
scholar	rs267608156
google	rs267608156
pharmgkb	rs267608156
gwascentral	rs267608156
openSNP	rs267608156
23andMe	rs267608156
SNPshot	rs267608156
SNPdbe	rs267608156
MSV3d	rs267608156
GWAS Ctlg	rs267608156

Max Magnitude

6

ClinVar
Risk	rs267608156(T;T)
Alt	rs267608156(T;T)
Reference	Rs267608156(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6029499dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076794.2,