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rs63751319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGAGACT;GGAGACT) 0 common in clinvar
(I;I) 0
Make rs63751319(-;-)
Make rs63751319(-;GGAGACT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806490
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs63751319
ebirs63751319
HLIrs63751319
Exacrs63751319
Varsomers63751319
Maprs63751319
PheGenIrs63751319
hapmaprs63751319
1000 genomesrs63751319
hgdprs63751319
ensemblrs63751319
gopubmedrs63751319
geneviewrs63751319
scholarrs63751319
googlers63751319
pharmgkbrs63751319
gwascentralrs63751319
openSNPrs63751319
23andMers63751319
23andMe allrs63751319
SNP Nexus

SNPshotrs63751319
SNPdbers63751319
MSV3drs63751319
GWAS Ctlgrs63751319
Max Magnitude0
ClinVar
Risk rs63751319(;)
Alt rs63751319(;)
Reference rs63751319(GGAGACT;GGAGACT)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033629_48033635delGGAGACT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074942.2, RCV000219135.1,