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rs1057520627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520627(G;T)
Make rs1057520627(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37048517
GeneMLH1
is asnp
is mentioned by
dbSNPrs1057520627
dbSNP (classic)rs1057520627
ClinGenrs1057520627
ebirs1057520627
HLIrs1057520627
Exacrs1057520627
Gnomadrs1057520627
Varsomers1057520627
LitVarrs1057520627
Maprs1057520627
PheGenIrs1057520627
Biobankrs1057520627
1000 genomesrs1057520627
hgdprs1057520627
ensemblrs1057520627
geneviewrs1057520627
scholarrs1057520627
googlers1057520627
pharmgkbrs1057520627
gwascentralrs1057520627
openSNPrs1057520627
23andMers1057520627
23andMe allrs1057520627
SNPshotrs1057520627
SNPdbers1057520627
MSV3drs1057520627
GWAS Ctlgrs1057520627
Max Magnitude0
ClinVar
Risk rs1057520627(T;T)
Alt rs1057520627(T;T)
Reference Rs1057520627(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37090008G>T
CLNSRC
CLNACC RCV000420036.1,