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rs148317871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148317871(A;A)
Make rs148317871(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050595
GeneMLH1
is asnp
is mentioned by
dbSNPrs148317871
ebirs148317871
HLIrs148317871
Exacrs148317871
Varsomers148317871
Maprs148317871
PheGenIrs148317871
hapmaprs148317871
1000 genomesrs148317871
hgdprs148317871
ensemblrs148317871
gopubmedrs148317871
geneviewrs148317871
scholarrs148317871
googlers148317871
pharmgkbrs148317871
gwascentralrs148317871
openSNPrs148317871
23andMers148317871
23andMe allrs148317871
SNP Nexus

SNPshotrs148317871
SNPdbers148317871
MSV3drs148317871
GWAS Ctlgrs148317871
Max Magnitude0
ClinVar
Risk rs148317871(A;A)
Alt rs148317871(A;A)
Reference rs148317871(G;G)
Significance Other
Disease Lynch syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37092086G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030221.3, RCV000160545.3,