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rs397508559

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508559(-;-)
Make rs397508559(-;AGTA)
Make rs397508559(AGTA;AGTA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614669
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508559
ebirs397508559
HLIrs397508559
Exacrs397508559
Varsomers397508559
Maprs397508559
PheGenIrs397508559
hapmaprs397508559
1000 genomesrs397508559
hgdprs397508559
ensemblrs397508559
gopubmedrs397508559
geneviewrs397508559
scholarrs397508559
googlers397508559
pharmgkbrs397508559
gwascentralrs397508559
openSNPrs397508559
23andMers397508559
23andMe allrs397508559
SNP Nexus

SNPshotrs397508559
SNPdbers397508559
MSV3drs397508559
GWAS Ctlgrs397508559
Max Magnitude0
ClinVar
Risk rs397508559(AGTA;AGTA)
Alt rs397508559(AGTA;AGTA)
Reference rs397508559(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254720_117254723dupAGTA
CLNSRC ClinVar
CLNACC RCV000046887.2,