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rs1057517541

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517541(C;T)
Make rs1057517541(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37025817
GeneMLH1
is asnp
is mentioned by
dbSNPrs1057517541
dbSNP (old)rs1057517541
ClinGenrs1057517541
ebirs1057517541
HLIrs1057517541
Exacrs1057517541
Gnomadrs1057517541
Varsomers1057517541
Maprs1057517541
PheGenIrs1057517541
Biobankrs1057517541
1000 genomesrs1057517541
hgdprs1057517541
ensemblrs1057517541
gopubmedrs1057517541
geneviewrs1057517541
scholarrs1057517541
googlers1057517541
pharmgkbrs1057517541
gwascentralrs1057517541
openSNPrs1057517541
23andMers1057517541
23andMe allrs1057517541
SNPshotrs1057517541
SNPdbers1057517541
MSV3drs1057517541
GWAS Ctlgrs1057517541
Max Magnitude0
ClinVar
Risk rs1057517541(T;T)
Alt rs1057517541(T;T)
Reference Rs1057517541(C;C)
Significance Pathogenic
Disease Lynch syndrome II Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome II Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37067308C>T
CLNSRC
CLNACC RCV000411311.1, RCV000464749.1, RCV000486818.1,