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rs397508147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508147(C;T)
Make rs397508147(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540269
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508147
ebirs397508147
HLIrs397508147
Exacrs397508147
Varsomers397508147
Maprs397508147
PheGenIrs397508147
hapmaprs397508147
1000 genomesrs397508147
hgdprs397508147
ensemblrs397508147
gopubmedrs397508147
geneviewrs397508147
scholarrs397508147
googlers397508147
pharmgkbrs397508147
gwascentralrs397508147
openSNPrs397508147
23andMers397508147
23andMe allrs397508147
SNP Nexus

SNPshotrs397508147
SNPdbers397508147
MSV3drs397508147
GWAS Ctlgrs397508147
Max Magnitude0
ClinVar
Risk rs397508147(T;T)
Alt rs397508147(T;T)
Reference rs397508147(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180323C>T
CLNSRC ClinVar
CLNACC RCV000046206.2,