rs267608148

Orientation

minus

Stabilized

minus

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

Make rs267608148(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

5999219

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs267608148
dbSNP (classic)	rs267608148
ClinGen	rs267608148
ebi	rs267608148
HLI	rs267608148
Exac	rs267608148
Gnomad	rs267608148
Varsome	rs267608148
LitVar	rs267608148
Map	rs267608148
PheGenI	rs267608148
Biobank	rs267608148
1000 genomes	rs267608148
hgdp	rs267608148
ensembl	rs267608148
geneview	rs267608148
scholar	rs267608148
google	rs267608148
pharmgkb	rs267608148
gwascentral	rs267608148
openSNP	rs267608148
23andMe	rs267608148
SNPshot	rs267608148
SNPdbe	rs267608148
MSV3d	rs267608148
GWAS Ctlg	rs267608148

Max Magnitude

6

ClinVar
Risk	rs267608148(T;T)
Alt	rs267608148(T;T)
Reference	Rs267608148(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6038851dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076878.2,