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rs397508487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs397508487(-;-)
Make rs397508487(-;AC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610571
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508487
ebirs397508487
HLIrs397508487
Exacrs397508487
Varsomers397508487
Maprs397508487
PheGenIrs397508487
hapmaprs397508487
1000 genomesrs397508487
hgdprs397508487
ensemblrs397508487
gopubmedrs397508487
geneviewrs397508487
scholarrs397508487
googlers397508487
pharmgkbrs397508487
gwascentralrs397508487
openSNPrs397508487
23andMers397508487
23andMe allrs397508487
SNP Nexus

SNPshotrs397508487
SNPdbers397508487
MSV3drs397508487
GWAS Ctlgrs397508487
Max Magnitude0
ClinVar
Risk rs397508487(;)
Alt rs397508487(;)
Reference rs397508487(AC;AC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250625_117250626delAC
CLNSRC ClinVar
CLNACC RCV000046768.2,