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rs397508720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508720(A;A)
Make rs397508720(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531076
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508720
ebirs397508720
HLIrs397508720
Exacrs397508720
Varsomers397508720
Maprs397508720
PheGenIrs397508720
hapmaprs397508720
1000 genomesrs397508720
hgdprs397508720
ensemblrs397508720
gopubmedrs397508720
geneviewrs397508720
scholarrs397508720
googlers397508720
pharmgkbrs397508720
gwascentralrs397508720
openSNPrs397508720
23andMers397508720
23andMe allrs397508720
SNP Nexus

SNPshotrs397508720
SNPdbers397508720
MSV3drs397508720
GWAS Ctlgrs397508720
Max Magnitude0
ClinVar
Risk rs397508720(A,T;A,T)
Alt rs397508720(A,T;A,T)
Reference rs397508720(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171130C>A; NC_000007.13:g.117171130C>T
CLNSRC ClinVar
CLNACC RCV000047142.2, RCV000047143.2,