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rs397508557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATG;ATG) 0 common in clinvar
Make rs397508557(-;-)
Make rs397508557(-;ATG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614663
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508557
ebirs397508557
HLIrs397508557
Exacrs397508557
Varsomers397508557
Maprs397508557
PheGenIrs397508557
hapmaprs397508557
1000 genomesrs397508557
hgdprs397508557
ensemblrs397508557
gopubmedrs397508557
geneviewrs397508557
scholarrs397508557
googlers397508557
pharmgkbrs397508557
gwascentralrs397508557
openSNPrs397508557
23andMers397508557
23andMe allrs397508557
SNP Nexus

SNPshotrs397508557
SNPdbers397508557
MSV3drs397508557
GWAS Ctlgrs397508557
Max Magnitude0
ClinVar
Risk rs397508557(;)
Alt rs397508557(;)
Reference rs397508557(ATG;ATG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254717_117254719delATG
CLNSRC ClinVar
CLNACC RCV000046885.2,