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rs397508269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508269(-;-)
Make rs397508269(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509037
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508269
ebirs397508269
HLIrs397508269
Exacrs397508269
Varsomers397508269
Maprs397508269
PheGenIrs397508269
hapmaprs397508269
1000 genomesrs397508269
hgdprs397508269
ensemblrs397508269
gopubmedrs397508269
geneviewrs397508269
scholarrs397508269
googlers397508269
pharmgkbrs397508269
gwascentralrs397508269
openSNPrs397508269
23andMers397508269
23andMe allrs397508269
SNP Nexus

SNPshotrs397508269
SNPdbers397508269
MSV3drs397508269
GWAS Ctlgrs397508269
Max Magnitude0
ClinVar
Risk rs397508269(;)
Alt rs397508269(;)
Reference rs397508269(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149091delA
CLNSRC ClinVar
CLNACC RCV000046424.2,