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rs397508466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508466(-;-)
Make rs397508466(-;A)
Make rs397508466(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117606733
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508466
ebirs397508466
HLIrs397508466
Exacrs397508466
Varsomers397508466
Maprs397508466
PheGenIrs397508466
hapmaprs397508466
1000 genomesrs397508466
hgdprs397508466
ensemblrs397508466
gopubmedrs397508466
geneviewrs397508466
scholarrs397508466
googlers397508466
pharmgkbrs397508466
gwascentralrs397508466
openSNPrs397508466
23andMers397508466
23andMe allrs397508466
SNP Nexus

SNPshotrs397508466
SNPdbers397508466
MSV3drs397508466
GWAS Ctlgrs397508466
Max Magnitude0
ClinVar
Risk rs397508466(A;A)
Alt rs397508466(A;A)
Reference rs397508466(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117246787dupA
CLNSRC ClinVar
CLNACC RCV000046734.2,