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rs397508254

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508254(-;-)
Make rs397508254(-;A)
Make rs397508254(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587814
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508254
ebirs397508254
HLIrs397508254
Exacrs397508254
Varsomers397508254
Maprs397508254
PheGenIrs397508254
hapmaprs397508254
1000 genomesrs397508254
hgdprs397508254
ensemblrs397508254
gopubmedrs397508254
geneviewrs397508254
scholarrs397508254
googlers397508254
pharmgkbrs397508254
gwascentralrs397508254
openSNPrs397508254
23andMers397508254
23andMe allrs397508254
SNP Nexus

SNPshotrs397508254
SNPdbers397508254
MSV3drs397508254
GWAS Ctlgrs397508254
Max Magnitude0
ClinVar
Risk rs397508254(A;A)
Alt rs397508254(A;A)
Reference rs397508254(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227868_117227869insA
CLNSRC ClinVar
CLNACC RCV000046396.2,