rs587781395

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;A)	6	Lynch syndrome
(A;A)	0	common in clinvar

Make rs587781395(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

5989877

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs587781395
dbSNP (classic)	rs587781395
ClinGen	rs587781395
ebi	rs587781395
HLI	rs587781395
Exac	rs587781395
Gnomad	rs587781395
Varsome	rs587781395
LitVar	rs587781395
Map	rs587781395
PheGenI	rs587781395
Biobank	rs587781395
1000 genomes	rs587781395
hgdp	rs587781395
ensembl	rs587781395
geneview	rs587781395
scholar	rs587781395
google	rs587781395
pharmgkb	rs587781395
gwascentral	rs587781395
openSNP	rs587781395
23andMe	rs587781395
SNPshot	rs587781395
SNPdbe	rs587781395
MSV3d	rs587781395
GWAS Ctlg	rs587781395

Max Magnitude

6

ClinVar
Risk	rs587781395(-;-)
Alt	rs587781395(-;-)
Reference	Rs587781395(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PMS2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000007.13:g.6029508delT
CLNSRC
CLNACC	RCV000129239.2, RCV000486460.1,