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rs397508569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508569(A;G)
Make rs397508569(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614706
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508569
ebirs397508569
HLIrs397508569
Exacrs397508569
Varsomers397508569
Maprs397508569
PheGenIrs397508569
hapmaprs397508569
1000 genomesrs397508569
hgdprs397508569
ensemblrs397508569
gopubmedrs397508569
geneviewrs397508569
scholarrs397508569
googlers397508569
pharmgkbrs397508569
gwascentralrs397508569
openSNPrs397508569
23andMers397508569
23andMe allrs397508569
SNP Nexus

SNPshotrs397508569
SNPdbers397508569
MSV3drs397508569
GWAS Ctlgrs397508569
Max Magnitude0
ClinVar
Risk rs397508569(G,T;G,T)
Alt rs397508569(G,T;G,T)
Reference rs397508569(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254760A>G
CLNSRC ClinVar
CLNACC RCV000046898.2,