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rs397508473

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATT;AATT) 0 common in clinvar
(ATTA;ATTA) 0 common in clinvar
Make rs397508473(-;-)
Make rs397508473(-;AATT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610527
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508473
ebirs397508473
HLIrs397508473
Exacrs397508473
Varsomers397508473
Maprs397508473
PheGenIrs397508473
hapmaprs397508473
1000 genomesrs397508473
hgdprs397508473
ensemblrs397508473
gopubmedrs397508473
geneviewrs397508473
scholarrs397508473
googlers397508473
pharmgkbrs397508473
gwascentralrs397508473
openSNPrs397508473
23andMers397508473
23andMe allrs397508473
SNP Nexus

SNPshotrs397508473
SNPdbers397508473
MSV3drs397508473
GWAS Ctlgrs397508473
Max Magnitude0
ClinVar
Risk rs397508473(;)
Alt rs397508473(;)
Reference rs397508473(ATTA;ATTA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250581_117250584delAATT
CLNSRC ClinVar
CLNACC RCV000046747.4,