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rs397508681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508681(-;-)
Make rs397508681(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665462
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508681
ebirs397508681
HLIrs397508681
Exacrs397508681
Varsomers397508681
Maprs397508681
PheGenIrs397508681
hapmaprs397508681
1000 genomesrs397508681
hgdprs397508681
ensemblrs397508681
gopubmedrs397508681
geneviewrs397508681
scholarrs397508681
googlers397508681
pharmgkbrs397508681
gwascentralrs397508681
openSNPrs397508681
23andMers397508681
23andMe allrs397508681
SNP Nexus

SNPshotrs397508681
SNPdbers397508681
MSV3drs397508681
GWAS Ctlgrs397508681
Max Magnitude0
ClinVar
Risk rs397508681(;)
Alt rs397508681(;)
Reference rs397508681(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305516delA
CLNSRC ClinVar
CLNACC RCV000047084.2,