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rs1064794122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome3
Position37017547
GeneMLH1
is asnp
is mentioned by
dbSNPrs1064794122
dbSNP (classic)rs1064794122
ClinGenrs1064794122
ebirs1064794122
HLIrs1064794122
Exacrs1064794122
Gnomadrs1064794122
Varsomers1064794122
LitVarrs1064794122
Maprs1064794122
PheGenIrs1064794122
Biobankrs1064794122
1000 genomesrs1064794122
hgdprs1064794122
ensemblrs1064794122
geneviewrs1064794122
scholarrs1064794122
googlers1064794122
pharmgkbrs1064794122
gwascentralrs1064794122
openSNPrs1064794122
23andMers1064794122
SNPshotrs1064794122
SNPdbers1064794122
MSV3drs1064794122
GWAS Ctlgrs1064794122
Max Magnitude0
ClinVar
Risk rs1064794122(-;-)
Alt rs1064794122(-;-)
Reference Rs1064794122(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37059038delA
CLNSRC
CLNACC RCV000484821.1,