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rs1060502940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1060502940(-;-)
Make rs1060502940(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47799316
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502940
dbSNP (classic)rs1060502940
ClinGenrs1060502940
ebirs1060502940
HLIrs1060502940
Exacrs1060502940
Gnomadrs1060502940
Varsomers1060502940
LitVarrs1060502940
Maprs1060502940
PheGenIrs1060502940
Biobankrs1060502940
1000 genomesrs1060502940
hgdprs1060502940
ensemblrs1060502940
geneviewrs1060502940
scholarrs1060502940
googlers1060502940
pharmgkbrs1060502940
gwascentralrs1060502940
openSNPrs1060502940
23andMers1060502940
23andMe allrs1060502940
SNPshotrs1060502940
SNPdbers1060502940
MSV3drs1060502940
GWAS Ctlgrs1060502940
Max Magnitude0
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,