rs1060502901

Orientation

plus

Stabilized

plus

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

Make rs1060502901(G;G)

Make rs1060502901(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47803435

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502901
dbSNP (classic)	rs1060502901
ClinGen	rs1060502901
ebi	rs1060502901
HLI	rs1060502901
Exac	rs1060502901
Gnomad	rs1060502901
Varsome	rs1060502901
LitVar	rs1060502901
Map	rs1060502901
PheGenI	rs1060502901
Biobank	rs1060502901
1000 genomes	rs1060502901
hgdp	rs1060502901
ensembl	rs1060502901
geneview	rs1060502901
scholar	rs1060502901
google	rs1060502901
pharmgkb	rs1060502901
gwascentral	rs1060502901
openSNP	rs1060502901
23andMe	rs1060502901
SNPshot	rs1060502901
SNPdbe	rs1060502901
MSV3d	rs1060502901
GWAS Ctlg	rs1060502901

Max Magnitude

0

ClinVar
Risk	rs1060502901(G;G)
Alt	rs1060502901(G;G)
Reference	Rs1060502901(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48030574T>G
CLNSRC
CLNACC	RCV000468032.1, RCV000491375.1,