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rs63751691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTTTCGAGGTG;GCTTTCGAGGTG) 0 common in clinvar
(TGGCTTTCGAGG;TGGCTTTCGAGG) 0 common in clinvar
Make rs63751691(-;-)
Make rs63751691(-;GCTTTCGAGGTG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001040
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751691
ebirs63751691
HLIrs63751691
Exacrs63751691
Varsomers63751691
Maprs63751691
PheGenIrs63751691
hapmaprs63751691
1000 genomesrs63751691
hgdprs63751691
ensemblrs63751691
gopubmedrs63751691
geneviewrs63751691
scholarrs63751691
googlers63751691
pharmgkbrs63751691
gwascentralrs63751691
openSNPrs63751691
23andMers63751691
23andMe allrs63751691
SNP Nexus

SNPshotrs63751691
SNPdbers63751691
MSV3drs63751691
GWAS Ctlgrs63751691
Max Magnitude0
ClinVar
Risk rs63751691(;)
Alt rs63751691(;)
Reference rs63751691(TGGCTTTCGAGG;TGGCTTTCGAGG)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042531_37042542delGCTTTCGAGGTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075616.2,