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rs1060500688

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500688(-;-)
Make rs1060500688(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37001015
GeneMLH1
is asnp
is mentioned by
dbSNPrs1060500688
dbSNP (old)rs1060500688
ClinGenrs1060500688
ebirs1060500688
HLIrs1060500688
Exacrs1060500688
Gnomadrs1060500688
Varsomers1060500688
Maprs1060500688
PheGenIrs1060500688
Biobankrs1060500688
1000 genomesrs1060500688
hgdprs1060500688
ensemblrs1060500688
gopubmedrs1060500688
geneviewrs1060500688
scholarrs1060500688
googlers1060500688
pharmgkbrs1060500688
gwascentralrs1060500688
openSNPrs1060500688
23andMers1060500688
23andMe allrs1060500688
SNPshotrs1060500688
SNPdbers1060500688
MSV3drs1060500688
GWAS Ctlgrs1060500688
Max Magnitude0
ClinVar
Risk rs1060500688(-;-)
Alt rs1060500688(-;-)
Reference Rs1060500688(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042506delG
CLNSRC
CLNACC RCV000460352.1,