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rs397508582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508582(C;T)
Make rs397508582(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627609
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508582
ebirs397508582
HLIrs397508582
Exacrs397508582
Varsomers397508582
Maprs397508582
PheGenIrs397508582
hapmaprs397508582
1000 genomesrs397508582
hgdprs397508582
ensemblrs397508582
gopubmedrs397508582
geneviewrs397508582
scholarrs397508582
googlers397508582
pharmgkbrs397508582
gwascentralrs397508582
openSNPrs397508582
23andMers397508582
23andMe allrs397508582
SNP Nexus

SNPshotrs397508582
SNPdbers397508582
MSV3drs397508582
GWAS Ctlgrs397508582
Max Magnitude0
ClinVar
Risk rs397508582(T;T)
Alt rs397508582(T;T)
Reference rs397508582(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267663C>T
CLNSRC ClinVar
CLNACC RCV000046926.2,