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rs397508234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508234(A;A)
Make rs397508234(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587730
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508234
ebirs397508234
HLIrs397508234
Exacrs397508234
Varsomers397508234
Maprs397508234
PheGenIrs397508234
hapmaprs397508234
1000 genomesrs397508234
hgdprs397508234
ensemblrs397508234
gopubmedrs397508234
geneviewrs397508234
scholarrs397508234
googlers397508234
pharmgkbrs397508234
gwascentralrs397508234
openSNPrs397508234
23andMers397508234
23andMe allrs397508234
SNP Nexus

SNPshotrs397508234
SNPdbers397508234
MSV3drs397508234
GWAS Ctlgrs397508234
Max Magnitude0
ClinVar
Risk rs397508234(A;A)
Alt rs397508234(A;A)
Reference rs397508234(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227784T>A
CLNSRC ClinVar
CLNACC RCV000046354.2,