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rs397508233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508233(A;G)
Make rs397508233(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587737
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508233
ebirs397508233
HLIrs397508233
Exacrs397508233
Varsomers397508233
Maprs397508233
PheGenIrs397508233
hapmaprs397508233
1000 genomesrs397508233
hgdprs397508233
ensemblrs397508233
gopubmedrs397508233
geneviewrs397508233
scholarrs397508233
googlers397508233
pharmgkbrs397508233
gwascentralrs397508233
openSNPrs397508233
23andMers397508233
23andMe allrs397508233
SNP Nexus

SNPshotrs397508233
SNPdbers397508233
MSV3drs397508233
GWAS Ctlgrs397508233
Max Magnitude0
ClinVar
Risk rs397508233(G;G)
Alt rs397508233(G;G)
Reference rs397508233(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227791A>G
CLNSRC ClinVar
CLNACC RCV000046352.2,