rs3209663

Orientation

minus

Stabilized

minus

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

Make rs3209663(A;A)

Make rs3209663(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

6005934

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs3209663
dbSNP (classic)	rs3209663
ClinGen	rs3209663
ebi	rs3209663
HLI	rs3209663
Exac	rs3209663
Gnomad	rs3209663
Varsome	rs3209663
LitVar	rs3209663
Map	rs3209663
PheGenI	rs3209663
Biobank	rs3209663
1000 genomes	rs3209663
hgdp	rs3209663
ensembl	rs3209663
geneview	rs3209663
scholar	rs3209663
google	rs3209663
pharmgkb	rs3209663
gwascentral	rs3209663
openSNP	rs3209663
23andMe	rs3209663
SNPshot	rs3209663
SNPdbe	rs3209663
MSV3d	rs3209663
GWAS Ctlg	rs3209663

Max Magnitude

6

ClinVar
Risk	rs3209663(A;A) rs3209663(T;T)
Alt	rs3209663(A;A) rs3209663(T;T)
Reference	Rs3209663(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6045565C>A
CLNSRC
CLNACC	RCV000203898.2,