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rs397508322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397508322(-;-)
Make rs397508322(-;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592086
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508322
ebirs397508322
HLIrs397508322
Exacrs397508322
Varsomers397508322
Maprs397508322
PheGenIrs397508322
hapmaprs397508322
1000 genomesrs397508322
hgdprs397508322
ensemblrs397508322
gopubmedrs397508322
geneviewrs397508322
scholarrs397508322
googlers397508322
pharmgkbrs397508322
gwascentralrs397508322
openSNPrs397508322
23andMers397508322
23andMe allrs397508322
SNP Nexus

SNPshotrs397508322
SNPdbers397508322
MSV3drs397508322
GWAS Ctlgrs397508322
Max Magnitude0
ClinVar
Risk rs397508322(;)
Alt rs397508322(;)
Reference rs397508322(TT;TT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232140_117232141delTT
CLNSRC ClinVar
CLNACC RCV000046507.2,