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rs397508324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508324(-;-)
Make rs397508324(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592148
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508324
ebirs397508324
HLIrs397508324
Exacrs397508324
Varsomers397508324
Maprs397508324
PheGenIrs397508324
hapmaprs397508324
1000 genomesrs397508324
hgdprs397508324
ensemblrs397508324
gopubmedrs397508324
geneviewrs397508324
scholarrs397508324
googlers397508324
pharmgkbrs397508324
gwascentralrs397508324
openSNPrs397508324
23andMers397508324
23andMe allrs397508324
SNP Nexus

SNPshotrs397508324
SNPdbers397508324
MSV3drs397508324
GWAS Ctlgrs397508324
Max Magnitude0
ClinVar
Risk rs397508324(;)
Alt rs397508324(;)
Reference rs397508324(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232202delA
CLNSRC ClinVar
CLNACC RCV000046513.2,