rs1060502876

Orientation

plus

Stabilized

plus

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

Make rs1060502876(A;A)

Make rs1060502876(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47800718

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502876
dbSNP (classic)	rs1060502876
ClinGen	rs1060502876
ebi	rs1060502876
HLI	rs1060502876
Exac	rs1060502876
Gnomad	rs1060502876
Varsome	rs1060502876
LitVar	rs1060502876
Map	rs1060502876
PheGenI	rs1060502876
Biobank	rs1060502876
1000 genomes	rs1060502876
hgdp	rs1060502876
ensembl	rs1060502876
geneview	rs1060502876
scholar	rs1060502876
google	rs1060502876
pharmgkb	rs1060502876
gwascentral	rs1060502876
openSNP	rs1060502876
23andMe	rs1060502876
SNPshot	rs1060502876
SNPdbe	rs1060502876
MSV3d	rs1060502876
GWAS Ctlg	rs1060502876

Max Magnitude

0

ClinVar
Risk	rs1060502876(A;A)
Alt	rs1060502876(A;A)
Reference	Rs1060502876(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027857G>A
CLNSRC
CLNACC	RCV000470184.1,