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rs397508524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508524(-;-)
Make rs397508524(-;A)
Make rs397508524(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611704
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508524
ebirs397508524
HLIrs397508524
Exacrs397508524
Varsomers397508524
Maprs397508524
PheGenIrs397508524
hapmaprs397508524
1000 genomesrs397508524
hgdprs397508524
ensemblrs397508524
gopubmedrs397508524
geneviewrs397508524
scholarrs397508524
googlers397508524
pharmgkbrs397508524
gwascentralrs397508524
openSNPrs397508524
23andMers397508524
23andMe allrs397508524
SNP Nexus

SNPshotrs397508524
SNPdbers397508524
MSV3drs397508524
GWAS Ctlgrs397508524
Max Magnitude0
ClinVar
Risk rs397508524(A;A)
Alt rs397508524(A;A)
Reference rs397508524(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251758dupA
CLNSRC ClinVar
CLNACC RCV000046840.2,