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rs397508732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508732(C;C)
Make rs397508732(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531116
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508732
ebirs397508732
HLIrs397508732
Exacrs397508732
Varsomers397508732
Maprs397508732
PheGenIrs397508732
hapmaprs397508732
1000 genomesrs397508732
hgdprs397508732
ensemblrs397508732
gopubmedrs397508732
geneviewrs397508732
scholarrs397508732
googlers397508732
pharmgkbrs397508732
gwascentralrs397508732
openSNPrs397508732
23andMers397508732
23andMe allrs397508732
SNP Nexus

SNPshotrs397508732
SNPdbers397508732
MSV3drs397508732
GWAS Ctlgrs397508732
Max Magnitude0
ClinVar
Risk rs397508732(C,G;C,G)
Alt rs397508732(C,G;C,G)
Reference rs397508732(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171170T>C; NC_000007.13:g.117171170T>G
CLNSRC ClinVar
CLNACC RCV000047160.2, RCV000047161.2,