rs1060502940

Orientation

plus

Stabilized

plus

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

Make rs1060502940(-;-)

Make rs1060502940(-;AG)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47799316

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502940
dbSNP (classic)	rs1060502940
ClinGen	rs1060502940
ebi	rs1060502940
HLI	rs1060502940
Exac	rs1060502940
Gnomad	rs1060502940
Varsome	rs1060502940
LitVar	rs1060502940
Map	rs1060502940
PheGenI	rs1060502940
Biobank	rs1060502940
1000 genomes	rs1060502940
hgdp	rs1060502940
ensembl	rs1060502940
geneview	rs1060502940
scholar	rs1060502940
google	rs1060502940
pharmgkb	rs1060502940
gwascentral	rs1060502940
openSNP	rs1060502940
23andMe	rs1060502940
SNPshot	rs1060502940
SNPdbe	rs1060502940
MSV3d	rs1060502940
GWAS Ctlg	rs1060502940

Max Magnitude

0

ClinVar
Risk	rs1060502940(-;-)
Alt	rs1060502940(-;-)
Reference	Rs1060502940(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026455_48026456delAG
CLNSRC
CLNACC	RCV000457061.1,