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rs397508733

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 carrier of a cystic fibrosis allele
Make rs397508733(A;A)
Make rs397508733(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position117531114
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508733
ebirs397508733
HLIrs397508733
Exacrs397508733
Varsomers397508733
Maprs397508733
PheGenIrs397508733
hapmaprs397508733
1000 genomesrs397508733
hgdprs397508733
ensemblrs397508733
gopubmedrs397508733
geneviewrs397508733
scholarrs397508733
googlers397508733
pharmgkbrs397508733
gwascentralrs397508733
openSNPrs397508733
23andMers397508733
23andMe allrs397508733
SNP Nexus

SNPshotrs397508733
SNPdbers397508733
MSV3drs397508733
GWAS Ctlgrs397508733
Max Magnitude3
ClinVar
Risk rs397508733(A;A)
Alt rs397508733(A;A)
Reference rs397508733(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171168G>A
CLNSRC
CLNACC RCV000047163.2,