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rs63751090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751090(-;-)
Make rs63751090(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799563
GeneMSH6
is asnp
is mentioned by
dbSNPrs63751090
ebirs63751090
HLIrs63751090
Exacrs63751090
Varsomers63751090
Maprs63751090
PheGenIrs63751090
hapmaprs63751090
1000 genomesrs63751090
hgdprs63751090
ensemblrs63751090
gopubmedrs63751090
geneviewrs63751090
scholarrs63751090
googlers63751090
pharmgkbrs63751090
gwascentralrs63751090
openSNPrs63751090
23andMers63751090
23andMe allrs63751090
SNP Nexus

SNPshotrs63751090
SNPdbers63751090
MSV3drs63751090
GWAS Ctlgrs63751090
Max Magnitude0
ClinVar
Risk rs63751090(;)
Alt rs63751090(;)
Reference rs63751090(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026702delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074666.2,