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rs397508273

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508273(A;A)
Make rs397508273(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590376
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508273
ebirs397508273
HLIrs397508273
Exacrs397508273
Varsomers397508273
Maprs397508273
PheGenIrs397508273
hapmaprs397508273
1000 genomesrs397508273
hgdprs397508273
ensemblrs397508273
gopubmedrs397508273
geneviewrs397508273
scholarrs397508273
googlers397508273
pharmgkbrs397508273
gwascentralrs397508273
openSNPrs397508273
23andMers397508273
23andMe allrs397508273
SNP Nexus

SNPshotrs397508273
SNPdbers397508273
MSV3drs397508273
GWAS Ctlgrs397508273
Max Magnitude0
ClinVar
Risk rs397508273(A;A)
Alt rs397508273(A;A)
Reference rs397508273(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230430T>A
CLNSRC ClinVar
CLNACC RCV000046430.2,