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rs397508583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508583(-;-)
Make rs397508583(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530982
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508583
ebirs397508583
HLIrs397508583
Exacrs397508583
Varsomers397508583
Maprs397508583
PheGenIrs397508583
hapmaprs397508583
1000 genomesrs397508583
hgdprs397508583
ensemblrs397508583
gopubmedrs397508583
geneviewrs397508583
scholarrs397508583
googlers397508583
pharmgkbrs397508583
gwascentralrs397508583
openSNPrs397508583
23andMers397508583
23andMe allrs397508583
SNP Nexus

SNPshotrs397508583
SNPdbers397508583
MSV3drs397508583
GWAS Ctlgrs397508583
Max Magnitude0
ClinVar
Risk rs397508583(;)
Alt rs397508583(;)
Reference rs397508583(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171036delC
CLNSRC ClinVar
CLNACC RCV000046927.2,