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rs397508313

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508313(C;C)
Make rs397508313(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592023
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508313
ebirs397508313
HLIrs397508313
Exacrs397508313
Varsomers397508313
Maprs397508313
PheGenIrs397508313
hapmaprs397508313
1000 genomesrs397508313
hgdprs397508313
ensemblrs397508313
gopubmedrs397508313
geneviewrs397508313
scholarrs397508313
googlers397508313
pharmgkbrs397508313
gwascentralrs397508313
openSNPrs397508313
23andMers397508313
23andMe allrs397508313
SNP Nexus

SNPshotrs397508313
SNPdbers397508313
MSV3drs397508313
GWAS Ctlgrs397508313
Max Magnitude0
ClinVar
Risk rs397508313(C;C)
Alt rs397508313(C;C)
Reference rs397508313(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232077T>C
CLNSRC ClinVar
CLNACC RCV000046495.2,