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rs1064794348

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTGT;TTGT) 0 common in clinvar
Chromosome3
Position36996652
GeneMLH1
is asnp
is mentioned by
dbSNPrs1064794348
dbSNP (classic)rs1064794348
ClinGenrs1064794348
ebirs1064794348
HLIrs1064794348
Exacrs1064794348
Gnomadrs1064794348
Varsomers1064794348
LitVarrs1064794348
Maprs1064794348
PheGenIrs1064794348
Biobankrs1064794348
1000 genomesrs1064794348
hgdprs1064794348
ensemblrs1064794348
geneviewrs1064794348
scholarrs1064794348
googlers1064794348
pharmgkbrs1064794348
gwascentralrs1064794348
openSNPrs1064794348
23andMers1064794348
SNPshotrs1064794348
SNPdbers1064794348
MSV3drs1064794348
GWAS Ctlgrs1064794348
Max Magnitude0
ClinVar
Risk rs1064794348(-;-)
Alt rs1064794348(-;-)
Reference Rs1064794348(TTGT;TTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37038143_37038146delTGTT
CLNSRC
CLNACC RCV000484343.1,