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rs397508705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508705(A;C)
Make rs397508705(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117666906
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508705
ebirs397508705
HLIrs397508705
Exacrs397508705
Varsomers397508705
Maprs397508705
PheGenIrs397508705
hapmaprs397508705
1000 genomesrs397508705
hgdprs397508705
ensemblrs397508705
gopubmedrs397508705
geneviewrs397508705
scholarrs397508705
googlers397508705
pharmgkbrs397508705
gwascentralrs397508705
openSNPrs397508705
23andMers397508705
23andMe allrs397508705
SNP Nexus

SNPshotrs397508705
SNPdbers397508705
MSV3drs397508705
GWAS Ctlgrs397508705
Max Magnitude0
ClinVar
Risk rs397508705(C;C)
Alt rs397508705(C;C)
Reference rs397508705(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117306960A>C
CLNSRC ClinVar
CLNACC RCV000047117.2,