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rs397508329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508329(-;-)
Make rs397508329(-;A)
Make rs397508329(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592176
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508329
ebirs397508329
HLIrs397508329
Exacrs397508329
Varsomers397508329
Maprs397508329
PheGenIrs397508329
hapmaprs397508329
1000 genomesrs397508329
hgdprs397508329
ensemblrs397508329
gopubmedrs397508329
geneviewrs397508329
scholarrs397508329
googlers397508329
pharmgkbrs397508329
gwascentralrs397508329
openSNPrs397508329
23andMers397508329
23andMe allrs397508329
SNP Nexus

SNPshotrs397508329
SNPdbers397508329
MSV3drs397508329
GWAS Ctlgrs397508329
Max Magnitude0
ClinVar
Risk rs397508329(A;A)
Alt rs397508329(A;A)
Reference rs397508329(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232231dupA
CLNSRC ClinVar
CLNACC RCV000046519.2,