rs587780064

Orientation

minus

Stabilized

minus

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

Make rs587780064(G;T)

Make rs587780064(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

5989956

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs587780064
dbSNP (classic)	rs587780064
ClinGen	rs587780064
ebi	rs587780064
HLI	rs587780064
Exac	rs587780064
Gnomad	rs587780064
Varsome	rs587780064
LitVar	rs587780064
Map	rs587780064
PheGenI	rs587780064
Biobank	rs587780064
1000 genomes	rs587780064
hgdp	rs587780064
ensembl	rs587780064
geneview	rs587780064
scholar	rs587780064
google	rs587780064
pharmgkb	rs587780064
gwascentral	rs587780064
openSNP	rs587780064
23andMe	rs587780064
SNPshot	rs587780064
SNPdbe	rs587780064
MSV3d	rs587780064
GWAS Ctlg	rs587780064

Max Magnitude

6

ClinVar
Risk	rs587780064(T;T)
Alt	rs587780064(T;T)
Reference	Rs587780064(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PMS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.6029587C>A
CLNSRC
CLNACC	RCV000115713.2,