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rs397508253

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508253(-;-)
Make rs397508253(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587810
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508253
ebirs397508253
HLIrs397508253
Exacrs397508253
Varsomers397508253
Maprs397508253
PheGenIrs397508253
hapmaprs397508253
1000 genomesrs397508253
hgdprs397508253
ensemblrs397508253
gopubmedrs397508253
geneviewrs397508253
scholarrs397508253
googlers397508253
pharmgkbrs397508253
gwascentralrs397508253
openSNPrs397508253
23andMers397508253
23andMe allrs397508253
SNP Nexus

SNPshotrs397508253
SNPdbers397508253
MSV3drs397508253
GWAS Ctlgrs397508253
Max Magnitude0
ClinVar
Risk rs397508253(;)
Alt rs397508253(;)
Reference rs397508253(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227864delA
CLNSRC ClinVar
CLNACC RCV000046392.2,