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rs397508657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508657(A;A)
Make rs397508657(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480097
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508657
ebirs397508657
HLIrs397508657
Exacrs397508657
Varsomers397508657
Maprs397508657
PheGenIrs397508657
hapmaprs397508657
1000 genomesrs397508657
hgdprs397508657
ensemblrs397508657
gopubmedrs397508657
geneviewrs397508657
scholarrs397508657
googlers397508657
pharmgkbrs397508657
gwascentralrs397508657
openSNPrs397508657
23andMers397508657
23andMe allrs397508657
SNP Nexus

SNPshotrs397508657
SNPdbers397508657
MSV3drs397508657
GWAS Ctlgrs397508657
Max Magnitude0
ClinVar
Risk rs397508657(A,T;A,T)
Alt rs397508657(A,T;A,T)
Reference rs397508657(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120151G>A; NC_000007.13:g.117120151G>T
CLNSRC ClinVar
CLNACC RCV000047052.2, RCV000047053.2,