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rs1060500698

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060500698(-;-)
Make rs1060500698(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37050641
GeneMLH1
is asnp
is mentioned by
dbSNPrs1060500698
dbSNP (old)rs1060500698
ClinGenrs1060500698
ebirs1060500698
HLIrs1060500698
Exacrs1060500698
Gnomadrs1060500698
Varsomers1060500698
Maprs1060500698
PheGenIrs1060500698
Biobankrs1060500698
1000 genomesrs1060500698
hgdprs1060500698
ensemblrs1060500698
gopubmedrs1060500698
geneviewrs1060500698
scholarrs1060500698
googlers1060500698
pharmgkbrs1060500698
gwascentralrs1060500698
openSNPrs1060500698
23andMers1060500698
23andMe allrs1060500698
SNPshotrs1060500698
SNPdbers1060500698
MSV3drs1060500698
GWAS Ctlgrs1060500698
Max Magnitude0
ClinVar
Risk rs1060500698(-;-)
Alt rs1060500698(-;-)
Reference Rs1060500698(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092132delT
CLNSRC
CLNACC RCV000463125.1,