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rs63751892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGGGTTATTCGGCGGCT;GGGGTTATTCGGCGGCT) 0 common in clinvar
(GGTTATTCGGCGGCTGG;GGTTATTCGGCGGCTGG) 0 common in clinvar
Make rs63751892(-;-)
Make rs63751892(-;GGTTATTCGGCGGCTGG)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993565
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63751892
ebirs63751892
HLIrs63751892
Exacrs63751892
Varsomers63751892
Maprs63751892
PheGenIrs63751892
hapmaprs63751892
1000 genomesrs63751892
hgdprs63751892
ensemblrs63751892
gopubmedrs63751892
geneviewrs63751892
scholarrs63751892
googlers63751892
pharmgkbrs63751892
gwascentralrs63751892
openSNPrs63751892
23andMers63751892
23andMe allrs63751892
SNP Nexus

SNPshotrs63751892
SNPdbers63751892
MSV3drs63751892
GWAS Ctlgrs63751892
Max Magnitude0
ClinVar
Risk rs63751892(;)
Alt rs63751892(;)
Reference rs63751892(GGGGTTATTCGGCGGCT;GGGGTTATTCGGCGGCT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035056_37035072del17
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075414.2,