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rs397508230

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508230(A;A)
Make rs397508230(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559656
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508230
ebirs397508230
HLIrs397508230
Exacrs397508230
Varsomers397508230
Maprs397508230
PheGenIrs397508230
hapmaprs397508230
1000 genomesrs397508230
hgdprs397508230
ensemblrs397508230
gopubmedrs397508230
geneviewrs397508230
scholarrs397508230
googlers397508230
pharmgkbrs397508230
gwascentralrs397508230
openSNPrs397508230
23andMers397508230
23andMe allrs397508230
SNP Nexus

SNPshotrs397508230
SNPdbers397508230
MSV3drs397508230
GWAS Ctlgrs397508230
Max Magnitude0
ClinVar
Risk rs397508230(A,T;A,T)
Alt rs397508230(A,T;A,T)
Reference rs397508230(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199710G>A; NC_000007.13:g.117199710G>T
CLNSRC ClinVar
CLNACC RCV000046346.2, RCV000046347.2,