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rs397508464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508464(A;C)
Make rs397508464(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530918
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508464
ebirs397508464
HLIrs397508464
Exacrs397508464
Varsomers397508464
Maprs397508464
PheGenIrs397508464
hapmaprs397508464
1000 genomesrs397508464
hgdprs397508464
ensemblrs397508464
gopubmedrs397508464
geneviewrs397508464
scholarrs397508464
googlers397508464
pharmgkbrs397508464
gwascentralrs397508464
openSNPrs397508464
23andMers397508464
23andMe allrs397508464
SNP Nexus

SNPshotrs397508464
SNPdbers397508464
MSV3drs397508464
GWAS Ctlgrs397508464
Max Magnitude0
ClinVar
Risk rs397508464(C,G;C,G)
Alt rs397508464(C,G;C,G)
Reference rs397508464(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170972A>C; NC_000007.13:g.117170972A>G
CLNSRC ClinVar
CLNACC RCV000046730.2, RCV000046731.2,