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rs397508665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508665(-;-)
Make rs397508665(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664766
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508665
ebirs397508665
HLIrs397508665
Exacrs397508665
Varsomers397508665
Maprs397508665
PheGenIrs397508665
hapmaprs397508665
1000 genomesrs397508665
hgdprs397508665
ensemblrs397508665
gopubmedrs397508665
geneviewrs397508665
scholarrs397508665
googlers397508665
pharmgkbrs397508665
gwascentralrs397508665
openSNPrs397508665
23andMers397508665
23andMe allrs397508665
SNP Nexus

SNPshotrs397508665
SNPdbers397508665
MSV3drs397508665
GWAS Ctlgrs397508665
Max Magnitude0
ClinVar
Risk rs397508665(;)
Alt rs397508665(;)
Reference rs397508665(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304820delC
CLNSRC ClinVar
CLNACC RCV000047062.2,