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rs397508655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATA;ATA) 0 common in clinvar
Make rs397508655(ATA;TT)
Make rs397508655(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664706
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508655
ebirs397508655
HLIrs397508655
Exacrs397508655
Varsomers397508655
Maprs397508655
PheGenIrs397508655
hapmaprs397508655
1000 genomesrs397508655
hgdprs397508655
ensemblrs397508655
gopubmedrs397508655
geneviewrs397508655
scholarrs397508655
googlers397508655
pharmgkbrs397508655
gwascentralrs397508655
openSNPrs397508655
23andMers397508655
23andMe allrs397508655
SNP Nexus

SNPshotrs397508655
SNPdbers397508655
MSV3drs397508655
GWAS Ctlgrs397508655
Max Magnitude0
ClinVar
Risk rs397508655(TT;TT)
Alt rs397508655(TT;TT)
Reference rs397508655(ATA;ATA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304760_117304762delATAinsTT
CLNSRC ClinVar
CLNACC RCV000047050.2,