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rs397508589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397508589(-;-)
Make rs397508589(-;AG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627671
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508589
ebirs397508589
HLIrs397508589
Exacrs397508589
Varsomers397508589
Maprs397508589
PheGenIrs397508589
hapmaprs397508589
1000 genomesrs397508589
hgdprs397508589
ensemblrs397508589
gopubmedrs397508589
geneviewrs397508589
scholarrs397508589
googlers397508589
pharmgkbrs397508589
gwascentralrs397508589
openSNPrs397508589
23andMers397508589
23andMe allrs397508589
SNP Nexus

SNPshotrs397508589
SNPdbers397508589
MSV3drs397508589
GWAS Ctlgrs397508589
Max Magnitude0
ClinVar
Risk rs397508589(;)
Alt rs397508589(;)
Reference rs397508589(AG;AG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267725_117267726delAG
CLNSRC ClinVar
CLNACC RCV000046939.2,