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rs397508278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508278(A;A)
Make rs397508278(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590380
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508278
ebirs397508278
HLIrs397508278
Exacrs397508278
Varsomers397508278
Maprs397508278
PheGenIrs397508278
hapmaprs397508278
1000 genomesrs397508278
hgdprs397508278
ensemblrs397508278
gopubmedrs397508278
geneviewrs397508278
scholarrs397508278
googlers397508278
pharmgkbrs397508278
gwascentralrs397508278
openSNPrs397508278
23andMers397508278
23andMe allrs397508278
SNP Nexus

SNPshotrs397508278
SNPdbers397508278
MSV3drs397508278
GWAS Ctlgrs397508278
Max Magnitude0
ClinVar
Risk rs397508278(A,C;A,C)
Alt rs397508278(A,C;A,C)
Reference rs397508278(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230434T>A
CLNSRC ClinVar
CLNACC RCV000046436.2,