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rs397508346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508346(C;T)
Make rs397508346(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592325
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508346
ebirs397508346
HLIrs397508346
Exacrs397508346
Varsomers397508346
Maprs397508346
PheGenIrs397508346
hapmaprs397508346
1000 genomesrs397508346
hgdprs397508346
ensemblrs397508346
gopubmedrs397508346
geneviewrs397508346
scholarrs397508346
googlers397508346
pharmgkbrs397508346
gwascentralrs397508346
openSNPrs397508346
23andMers397508346
23andMe allrs397508346
SNP Nexus

SNPshotrs397508346
SNPdbers397508346
MSV3drs397508346
GWAS Ctlgrs397508346
Max Magnitude0
ClinVar
Risk rs397508346(T;T)
Alt rs397508346(T;T)
Reference rs397508346(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232379C>T
CLNSRC ClinVar
CLNACC RCV000046544.2,