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rs63751639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGAAA;GGAAA) 0 common in clinvar
(I;I) 0
Make rs63751639(-;-)
Make rs63751639(-;GGAAA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047671
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751639
ebirs63751639
HLIrs63751639
Exacrs63751639
Varsomers63751639
Maprs63751639
PheGenIrs63751639
hapmaprs63751639
1000 genomesrs63751639
hgdprs63751639
ensemblrs63751639
gopubmedrs63751639
geneviewrs63751639
scholarrs63751639
googlers63751639
pharmgkbrs63751639
gwascentralrs63751639
openSNPrs63751639
23andMers63751639
23andMe allrs63751639
SNP Nexus

SNPshotrs63751639
SNPdbers63751639
MSV3drs63751639
GWAS Ctlgrs63751639
Max Magnitude0
ClinVar
Risk rs63751639(;)
Alt rs63751639(;)
Reference rs63751639(GGAAA;GGAAA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089162_37089166delGGAAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075401.2,