rs1060503142

Orientation

minus

Stabilized

minus

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

Make rs1060503142(A;T)

Make rs1060503142(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

5987417

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs1060503142
dbSNP (classic)	rs1060503142
ClinGen	rs1060503142
ebi	rs1060503142
HLI	rs1060503142
Exac	rs1060503142
Gnomad	rs1060503142
Varsome	rs1060503142
LitVar	rs1060503142
Map	rs1060503142
PheGenI	rs1060503142
Biobank	rs1060503142
1000 genomes	rs1060503142
hgdp	rs1060503142
ensembl	rs1060503142
geneview	rs1060503142
scholar	rs1060503142
google	rs1060503142
pharmgkb	rs1060503142
gwascentral	rs1060503142
openSNP	rs1060503142
23andMe	rs1060503142
SNPshot	rs1060503142
SNPdbe	rs1060503142
MSV3d	rs1060503142
GWAS Ctlg	rs1060503142

Max Magnitude

0

ClinVar
Risk	rs1060503142(T;T)
Alt	rs1060503142(T;T)
Reference	Rs1060503142(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	PMS2
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000007.13:g.6027048T>A
CLNSRC
CLNACC	RCV000466795.1,