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rs397508281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397508281(-;-)
Make rs397508281(-;AG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590386
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508281
dbSNP (old)rs397508281
ClinGenrs397508281
ebirs397508281
HLIrs397508281
Exacrs397508281
Gnomadrs397508281
Varsomers397508281
Maprs397508281
PheGenIrs397508281
Biobankrs397508281
1000 genomesrs397508281
hgdprs397508281
ensemblrs397508281
gopubmedrs397508281
geneviewrs397508281
scholarrs397508281
googlers397508281
pharmgkbrs397508281
gwascentralrs397508281
openSNPrs397508281
23andMers397508281
23andMe allrs397508281
SNP Nexus

SNPshotrs397508281
SNPdbers397508281
MSV3drs397508281
GWAS Ctlgrs397508281
Max Magnitude0
ClinVar
Risk rs397508281(-;-)
Alt rs397508281(-;-)
Reference Rs397508281(AG;AG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230440_117230441delAG
CLNSRC ClinVar
CLNACC RCV000046439.2,