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rs150766139

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150766139(A;A)
Make rs150766139(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position2046238
GeneNTHL1, TSC2
is asnp
is mentioned by
dbSNPrs150766139
ebirs150766139
HLIrs150766139
Exacrs150766139
Varsomers150766139
Maprs150766139
PheGenIrs150766139
hapmaprs150766139
1000 genomesrs150766139
hgdprs150766139
ensemblrs150766139
gopubmedrs150766139
geneviewrs150766139
scholarrs150766139
googlers150766139
pharmgkbrs150766139
gwascentralrs150766139
openSNPrs150766139
23andMers150766139
23andMe allrs150766139
SNP Nexus

SNPshotrs150766139
SNPdbers150766139
MSV3drs150766139
GWAS Ctlgrs150766139
Max Magnitude0
ClinVar
Risk rs150766139(A;A)
Alt rs150766139(A;A)
Reference rs150766139(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 3
Variation info
Gene NTHL1 TSC2
CLNDBN Familial adenomatous polyposis 3
Reversed 0
HGVS NC_000016.9:g.2096239G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172911.3,