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rs1064793177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position37049003
GeneMLH1
is asnp
is mentioned by
dbSNPrs1064793177
dbSNP (old)rs1064793177
ClinGenrs1064793177
ebirs1064793177
HLIrs1064793177
Exacrs1064793177
Gnomadrs1064793177
Varsomers1064793177
LitVarrs1064793177
Maprs1064793177
PheGenIrs1064793177
Biobankrs1064793177
1000 genomesrs1064793177
hgdprs1064793177
ensemblrs1064793177
gopubmedrs1064793177
geneviewrs1064793177
scholarrs1064793177
googlers1064793177
pharmgkbrs1064793177
gwascentralrs1064793177
openSNPrs1064793177
23andMers1064793177
23andMe allrs1064793177
SNPshotrs1064793177
SNPdbers1064793177
MSV3drs1064793177
GWAS Ctlgrs1064793177
Max Magnitude0
ClinVar
Risk rs1064793177(-;-)
Alt rs1064793177(-;-)
Reference Rs1064793177(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37090494delC
CLNSRC
CLNACC RCV000484128.1,