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rs372946560

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372946560(C;T)
Make rs372946560(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2043566
GeneNTHL1
is asnp
is mentioned by
dbSNPrs372946560
ebirs372946560
HLIrs372946560
Exacrs372946560
Varsomers372946560
Maprs372946560
PheGenIrs372946560
hapmaprs372946560
1000 genomesrs372946560
hgdprs372946560
ensemblrs372946560
gopubmedrs372946560
geneviewrs372946560
scholarrs372946560
googlers372946560
pharmgkbrs372946560
gwascentralrs372946560
openSNPrs372946560
23andMers372946560
23andMe allrs372946560
SNP Nexus

SNPshotrs372946560
SNPdbers372946560
MSV3drs372946560
GWAS Ctlgrs372946560
Max Magnitude0
ClinVar
Risk rs372946560(T;T)
Alt rs372946560(T;T)
Reference rs372946560(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 3
Variation info
Gene NTHL1
CLNDBN Familial adenomatous polyposis 3
Reversed 0
HGVS NC_000016.9:g.2093567C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202319.3,