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rs397508588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508588(A;A)
Make rs397508588(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627670
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508588
ebirs397508588
HLIrs397508588
Exacrs397508588
Varsomers397508588
Maprs397508588
PheGenIrs397508588
hapmaprs397508588
1000 genomesrs397508588
hgdprs397508588
ensemblrs397508588
gopubmedrs397508588
geneviewrs397508588
scholarrs397508588
googlers397508588
pharmgkbrs397508588
gwascentralrs397508588
openSNPrs397508588
23andMers397508588
23andMe allrs397508588
SNP Nexus

SNPshotrs397508588
SNPdbers397508588
MSV3drs397508588
GWAS Ctlgrs397508588
Max Magnitude0
ClinVar
Risk rs397508588(A;A) rs397508588(G;G)
Alt rs397508588(A;A) rs397508588(G;G)
Reference Rs397508588(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267724C>A; NC_000007.13:g.117267724C>G
CLNSRC ClinVar
CLNACC RCV000046937.2, RCV000046938.2,