rs1060503137

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(AT;AT)	0	common in clinvar

Make rs1060503137(-;-)

Make rs1060503137(-;AT)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

5986900

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs1060503137
dbSNP (classic)	rs1060503137
ClinGen	rs1060503137
ebi	rs1060503137
HLI	rs1060503137
Exac	rs1060503137
Gnomad	rs1060503137
Varsome	rs1060503137
LitVar	rs1060503137
Map	rs1060503137
PheGenI	rs1060503137
Biobank	rs1060503137
1000 genomes	rs1060503137
hgdp	rs1060503137
ensembl	rs1060503137
geneview	rs1060503137
scholar	rs1060503137
google	rs1060503137
pharmgkb	rs1060503137
gwascentral	rs1060503137
openSNP	rs1060503137
23andMe	rs1060503137
SNPshot	rs1060503137
SNPdbe	rs1060503137
MSV3d	rs1060503137
GWAS Ctlg	rs1060503137

Max Magnitude

0

ClinVar
Risk	rs1060503137(-;-)
Alt	rs1060503137(-;-)
Reference	Rs1060503137(AT;AT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6026531_6026532delAT
CLNSRC
CLNACC	RCV000469787.1,