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rs397508179

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508179(A;C)
Make rs397508179(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548639
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508179
ebirs397508179
HLIrs397508179
Exacrs397508179
Varsomers397508179
Maprs397508179
PheGenIrs397508179
hapmaprs397508179
1000 genomesrs397508179
hgdprs397508179
ensemblrs397508179
gopubmedrs397508179
geneviewrs397508179
scholarrs397508179
googlers397508179
pharmgkbrs397508179
gwascentralrs397508179
openSNPrs397508179
23andMers397508179
23andMe allrs397508179
SNP Nexus

SNPshotrs397508179
SNPdbers397508179
MSV3drs397508179
GWAS Ctlgrs397508179
Max Magnitude0
ClinVar
Risk rs397508179(C;C)
Alt rs397508179(C;C)
Reference rs397508179(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188693A>C
CLNSRC ClinVar
CLNACC RCV000046262.2,