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rs397508320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508320(C;T)
Make rs397508320(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592076
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508320
ebirs397508320
HLIrs397508320
Exacrs397508320
Varsomers397508320
Maprs397508320
PheGenIrs397508320
hapmaprs397508320
1000 genomesrs397508320
hgdprs397508320
ensemblrs397508320
gopubmedrs397508320
geneviewrs397508320
scholarrs397508320
googlers397508320
pharmgkbrs397508320
gwascentralrs397508320
openSNPrs397508320
23andMers397508320
23andMe allrs397508320
SNP Nexus

SNPshotrs397508320
SNPdbers397508320
MSV3drs397508320
GWAS Ctlgrs397508320
Max Magnitude0
ClinVar
Risk rs397508320(T;T)
Alt rs397508320(T;T)
Reference rs397508320(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232130C>T
CLNSRC ClinVar
CLNACC RCV000046504.2,