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rs397508486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508486(-;-)
Make rs397508486(-;A)
Make rs397508486(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530928
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508486
ebirs397508486
HLIrs397508486
Exacrs397508486
Varsomers397508486
Maprs397508486
PheGenIrs397508486
hapmaprs397508486
1000 genomesrs397508486
hgdprs397508486
ensemblrs397508486
gopubmedrs397508486
geneviewrs397508486
scholarrs397508486
googlers397508486
pharmgkbrs397508486
gwascentralrs397508486
openSNPrs397508486
23andMers397508486
23andMe allrs397508486
SNP Nexus

SNPshotrs397508486
SNPdbers397508486
MSV3drs397508486
GWAS Ctlgrs397508486
Max Magnitude0
ClinVar
Risk rs397508486(A;A)
Alt rs397508486(A;A)
Reference rs397508486(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170982dupA
CLNSRC ClinVar
CLNACC RCV000046766.2,