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rs397508547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508547(A;A)
Make rs397508547(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614612
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508547
ebirs397508547
HLIrs397508547
Exacrs397508547
Varsomers397508547
Maprs397508547
PheGenIrs397508547
hapmaprs397508547
1000 genomesrs397508547
hgdprs397508547
ensemblrs397508547
gopubmedrs397508547
geneviewrs397508547
scholarrs397508547
googlers397508547
pharmgkbrs397508547
gwascentralrs397508547
openSNPrs397508547
23andMers397508547
23andMe allrs397508547
SNP Nexus

SNPshotrs397508547
SNPdbers397508547
MSV3drs397508547
GWAS Ctlgrs397508547
Max Magnitude0
ClinVar
Risk rs397508547(A;A)
Alt rs397508547(A;A)
Reference rs397508547(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254666G>A
CLNSRC ClinVar
CLNACC RCV000046875.2,