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rs63750196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750196(-;-)
Make rs63750196(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803429
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750196
ebirs63750196
HLIrs63750196
Exacrs63750196
Varsomers63750196
Maprs63750196
PheGenIrs63750196
hapmaprs63750196
1000 genomesrs63750196
hgdprs63750196
ensemblrs63750196
gopubmedrs63750196
geneviewrs63750196
scholarrs63750196
googlers63750196
pharmgkbrs63750196
gwascentralrs63750196
openSNPrs63750196
23andMers63750196
23andMe allrs63750196
SNP Nexus

SNPshotrs63750196
SNPdbers63750196
MSV3drs63750196
GWAS Ctlgrs63750196
Max Magnitude0
ClinVar
Risk rs63750196(;)
Alt rs63750196(;)
Reference rs63750196(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030568delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074814.2,