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rs397508372

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508372(-;-)
Make rs397508372(-;C)
Make rs397508372(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592557
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508372
ebirs397508372
HLIrs397508372
Exacrs397508372
Varsomers397508372
Maprs397508372
PheGenIrs397508372
hapmaprs397508372
1000 genomesrs397508372
hgdprs397508372
ensemblrs397508372
gopubmedrs397508372
geneviewrs397508372
scholarrs397508372
googlers397508372
pharmgkbrs397508372
gwascentralrs397508372
openSNPrs397508372
23andMers397508372
23andMe allrs397508372
SNP Nexus

SNPshotrs397508372
SNPdbers397508372
MSV3drs397508372
GWAS Ctlgrs397508372
Max Magnitude0
ClinVar
Risk rs397508372(C;C)
Alt rs397508372(C;C)
Reference rs397508372(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232612dupC
CLNSRC ClinVar
CLNACC RCV000046587.2,