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rs1060500703

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060500703(-;-)
Make rs1060500703(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37025641
GeneMLH1
is asnp
is mentioned by
dbSNPrs1060500703
dbSNP (old)rs1060500703
ClinGenrs1060500703
ebirs1060500703
HLIrs1060500703
Exacrs1060500703
Gnomadrs1060500703
Varsomers1060500703
Maprs1060500703
PheGenIrs1060500703
Biobankrs1060500703
1000 genomesrs1060500703
hgdprs1060500703
ensemblrs1060500703
gopubmedrs1060500703
geneviewrs1060500703
scholarrs1060500703
googlers1060500703
pharmgkbrs1060500703
gwascentralrs1060500703
openSNPrs1060500703
23andMers1060500703
23andMe allrs1060500703
SNPshotrs1060500703
SNPdbers1060500703
MSV3drs1060500703
GWAS Ctlgrs1060500703
Max Magnitude0
ClinVar
Risk rs1060500703(-;-)
Alt rs1060500703(-;-)
Reference Rs1060500703(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067132delT
CLNSRC
CLNACC RCV000469473.1,