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rs397508458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508458(-;-)
Make rs397508458(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117606674
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508458
ebirs397508458
HLIrs397508458
Exacrs397508458
Varsomers397508458
Maprs397508458
PheGenIrs397508458
hapmaprs397508458
1000 genomesrs397508458
hgdprs397508458
ensemblrs397508458
gopubmedrs397508458
geneviewrs397508458
scholarrs397508458
googlers397508458
pharmgkbrs397508458
gwascentralrs397508458
openSNPrs397508458
23andMers397508458
23andMe allrs397508458
SNP Nexus

SNPshotrs397508458
SNPdbers397508458
MSV3drs397508458
GWAS Ctlgrs397508458
Max Magnitude0
ClinVar
Risk rs397508458(;)
Alt rs397508458(;)
Reference rs397508458(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117246728delG
CLNSRC ClinVar
CLNACC RCV000046719.2,