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rs397508484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508484(C;C)
Make rs397508484(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530927
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508484
ebirs397508484
HLIrs397508484
Exacrs397508484
Varsomers397508484
Maprs397508484
PheGenIrs397508484
hapmaprs397508484
1000 genomesrs397508484
hgdprs397508484
ensemblrs397508484
gopubmedrs397508484
geneviewrs397508484
scholarrs397508484
googlers397508484
pharmgkbrs397508484
gwascentralrs397508484
openSNPrs397508484
23andMers397508484
23andMe allrs397508484
SNP Nexus

SNPshotrs397508484
SNPdbers397508484
MSV3drs397508484
GWAS Ctlgrs397508484
Max Magnitude0
ClinVar
Risk rs397508484(C,G;C,G)
Alt rs397508484(C,G;C,G)
Reference rs397508484(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170981T>C; NC_000007.13:g.117170981T>G
CLNSRC ClinVar
CLNACC RCV000046761.2, RCV000046762.2,