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rs397508475

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508475(-;-)
Make rs397508475(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610528
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508475
ebirs397508475
HLIrs397508475
Exacrs397508475
Varsomers397508475
Maprs397508475
PheGenIrs397508475
hapmaprs397508475
1000 genomesrs397508475
hgdprs397508475
ensemblrs397508475
gopubmedrs397508475
geneviewrs397508475
scholarrs397508475
googlers397508475
pharmgkbrs397508475
gwascentralrs397508475
openSNPrs397508475
23andMers397508475
23andMe allrs397508475
SNP Nexus

SNPshotrs397508475
SNPdbers397508475
MSV3drs397508475
GWAS Ctlgrs397508475
Max Magnitude0
ClinVar
Risk rs397508475(;)
Alt rs397508475(;)
Reference rs397508475(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250582delA
CLNSRC ClinVar
CLNACC RCV000046749.2,