rs1060502946

Orientation

plus

Stabilized

plus

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

Make rs1060502946(-;AA)

Make rs1060502946(AA;AA)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47799278

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502946
dbSNP (classic)	rs1060502946
ClinGen	rs1060502946
ebi	rs1060502946
HLI	rs1060502946
Exac	rs1060502946
Gnomad	rs1060502946
Varsome	rs1060502946
LitVar	rs1060502946
Map	rs1060502946
PheGenI	rs1060502946
Biobank	rs1060502946
1000 genomes	rs1060502946
hgdp	rs1060502946
ensembl	rs1060502946
geneview	rs1060502946
scholar	rs1060502946
google	rs1060502946
pharmgkb	rs1060502946
gwascentral	rs1060502946
openSNP	rs1060502946
23andMe	rs1060502946
SNPshot	rs1060502946
SNPdbe	rs1060502946
MSV3d	rs1060502946
GWAS Ctlg	rs1060502946

Max Magnitude

0

ClinVar
Risk	rs1060502946(AA;AA)
Alt	rs1060502946(AA;AA)
Reference	Rs1060502946(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026417_48026418insAA
CLNSRC
CLNACC	RCV000462324.1,