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rs397508667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAG;TAG) 0 common in clinvar
Make rs397508667(AA;AA)
Make rs397508667(AA;TAG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664795
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508667
ebirs397508667
HLIrs397508667
Exacrs397508667
Varsomers397508667
Maprs397508667
PheGenIrs397508667
hapmaprs397508667
1000 genomesrs397508667
hgdprs397508667
ensemblrs397508667
gopubmedrs397508667
geneviewrs397508667
scholarrs397508667
googlers397508667
pharmgkbrs397508667
gwascentralrs397508667
openSNPrs397508667
23andMers397508667
23andMe allrs397508667
SNP Nexus

SNPshotrs397508667
SNPdbers397508667
MSV3drs397508667
GWAS Ctlgrs397508667
Max Magnitude0
ClinVar
Risk rs397508667(AA;AA)
Alt rs397508667(AA;AA)
Reference rs397508667(TAG;TAG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304849_117304851delTAGinsAA
CLNSRC ClinVar
CLNACC RCV000047067.2,