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rs63751301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGAG;GGAG) 0 common in clinvar
(GGGA;GGGA) 0 common in clinvar
(I;I) 0
Make rs63751301(-;-)
Make rs63751301(-;GGGA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048573
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751301
ebirs63751301
HLIrs63751301
Exacrs63751301
Varsomers63751301
Maprs63751301
PheGenIrs63751301
hapmaprs63751301
1000 genomesrs63751301
hgdprs63751301
ensemblrs63751301
gopubmedrs63751301
geneviewrs63751301
scholarrs63751301
googlers63751301
pharmgkbrs63751301
gwascentralrs63751301
openSNPrs63751301
23andMers63751301
23andMe allrs63751301
SNP Nexus

SNPshotrs63751301
SNPdbers63751301
MSV3drs63751301
GWAS Ctlgrs63751301
Max Magnitude0
ClinVar
Risk rs63751301(;)
Alt rs63751301(;)
Reference rs63751301(GGAG;GGAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090064_37090067delGGGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075436.2,