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rs397508554

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508554(A;T)
Make rs397508554(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530965
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508554
ebirs397508554
HLIrs397508554
Exacrs397508554
Varsomers397508554
Maprs397508554
PheGenIrs397508554
hapmaprs397508554
1000 genomesrs397508554
hgdprs397508554
ensemblrs397508554
gopubmedrs397508554
geneviewrs397508554
scholarrs397508554
googlers397508554
pharmgkbrs397508554
gwascentralrs397508554
openSNPrs397508554
23andMers397508554
23andMe allrs397508554
SNP Nexus

SNPshotrs397508554
SNPdbers397508554
MSV3drs397508554
GWAS Ctlgrs397508554
Max Magnitude0
ClinVar
Risk rs397508554(T;T)
Alt rs397508554(T;T)
Reference rs397508554(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171019A>T
CLNSRC ClinVar
CLNACC RCV000046882.2,