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rs397508533

From SNPedia

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Geno Mag Summary
(A;G) 3 carrier of a cystic fibrosis allele
(G;G) 0 common in clinvar
Make rs397508533(C;C)
Make rs397508533(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117611735
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508533
ebirs397508533
HLIrs397508533
Exacrs397508533
Varsomers397508533
Maprs397508533
PheGenIrs397508533
hapmaprs397508533
1000 genomesrs397508533
hgdprs397508533
ensemblrs397508533
gopubmedrs397508533
geneviewrs397508533
scholarrs397508533
googlers397508533
pharmgkbrs397508533
gwascentralrs397508533
openSNPrs397508533
23andMers397508533
23andMe allrs397508533
SNP Nexus

SNPshotrs397508533
SNPdbers397508533
MSV3drs397508533
GWAS Ctlgrs397508533
Max Magnitude3
ClinVar
Risk rs397508533(C;C)
Alt rs397508533(C;C)
Reference rs397508533(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251789G>A; NC_000007.13:g.117251789G>C
CLNSRC CFTR2
CLNACC RCV000191002.1, RCV000046856.2,