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rs1064793671

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position47800845
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064793671
dbSNP (old)rs1064793671
ClinGenrs1064793671
ebirs1064793671
HLIrs1064793671
Exacrs1064793671
Gnomadrs1064793671
Varsomers1064793671
Maprs1064793671
PheGenIrs1064793671
Biobankrs1064793671
1000 genomesrs1064793671
hgdprs1064793671
ensemblrs1064793671
gopubmedrs1064793671
geneviewrs1064793671
scholarrs1064793671
googlers1064793671
pharmgkbrs1064793671
gwascentralrs1064793671
openSNPrs1064793671
23andMers1064793671
23andMe allrs1064793671
SNPshotrs1064793671
SNPdbers1064793671
MSV3drs1064793671
GWAS Ctlgrs1064793671
Max Magnitude0
ClinVar
Risk rs1064793671(G;G)
Alt rs1064793671(G;G)
Reference Rs1064793671(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027984C>G
CLNSRC
CLNACC RCV000480127.1,