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rs35502531

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs35502531(AA;GC)
Make rs35502531(GC;GC)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047639
GeneMLH1
is asnp
is mentioned by
dbSNPrs35502531
ebirs35502531
HLIrs35502531
Exacrs35502531
Varsomers35502531
Maprs35502531
PheGenIrs35502531
hapmaprs35502531
1000 genomesrs35502531
hgdprs35502531
ensemblrs35502531
gopubmedrs35502531
geneviewrs35502531
scholarrs35502531
googlers35502531
pharmgkbrs35502531
gwascentralrs35502531
openSNPrs35502531
23andMers35502531
23andMe allrs35502531
SNP Nexus

SNPshotrs35502531
SNPdbers35502531
MSV3drs35502531
GWAS Ctlgrs35502531
Max Magnitude0
OMIM120436
Desc
Variant0012
Relatedalso
ClinVar
Risk rs35502531(GC;GC)
Alt rs35502531(GC;GC)
Reference rs35502531(AA;AA)
Significance Other
Disease Lynch syndrome II not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I
Variation info
Gene MLH1
CLNDBN Lynch syndrome II not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I
Reversed 0
HGVS NC_000003.11:g.37089130_37089131delAAinsGC
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000018620.4, RCV000034542.1, RCV000075382.3, RCV000121363.2, RCV000130907.5, RCV000144600.1,