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rs1064793172

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position37014509
GeneMLH1
is asnp
is mentioned by
dbSNPrs1064793172
dbSNP (old)rs1064793172
ClinGenrs1064793172
ebirs1064793172
HLIrs1064793172
Exacrs1064793172
Gnomadrs1064793172
Varsomers1064793172
Maprs1064793172
PheGenIrs1064793172
Biobankrs1064793172
1000 genomesrs1064793172
hgdprs1064793172
ensemblrs1064793172
gopubmedrs1064793172
geneviewrs1064793172
scholarrs1064793172
googlers1064793172
pharmgkbrs1064793172
gwascentralrs1064793172
openSNPrs1064793172
23andMers1064793172
23andMe allrs1064793172
SNPshotrs1064793172
SNPdbers1064793172
MSV3drs1064793172
GWAS Ctlgrs1064793172
Max Magnitude0
ClinVar
Risk rs1064793172(-;-)
Alt rs1064793172(-;-)
Reference Rs1064793172(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37056000delC
CLNSRC
CLNACC RCV000485005.1,