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rs35001569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs35001569(A;G)
Make rs35001569(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047639
GeneMLH1
is asnp
is mentioned by
dbSNPrs35001569
ebirs35001569
HLIrs35001569
Exacrs35001569
Varsomers35001569
Maprs35001569
PheGenIrs35001569
hapmaprs35001569
1000 genomesrs35001569
hgdprs35001569
ensemblrs35001569
gopubmedrs35001569
geneviewrs35001569
scholarrs35001569
googlers35001569
pharmgkbrs35001569
gwascentralrs35001569
openSNPrs35001569
23andMers35001569
23andMe allrs35001569
SNP Nexus

SNPshotrs35001569
SNPdbers35001569
MSV3drs35001569
GWAS Ctlgrs35001569
GMAF0.004132
Max Magnitude0
ClinVar
Risk rs35001569(G,T;G,T)
Alt rs35001569(G,T;G,T)
Reference rs35001569(A;A)
Significance Other
Disease Lynch syndrome not provided Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37089130A>G; NC_000003.11:g.37089130A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075380.2, RCV000114852.3, RCV000132423.4, RCV000174992.2, RCV000075381.2,