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rs397508528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508528(A;A)
Make rs397508528(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530952
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508528
ebirs397508528
HLIrs397508528
Exacrs397508528
Varsomers397508528
Maprs397508528
PheGenIrs397508528
hapmaprs397508528
1000 genomesrs397508528
hgdprs397508528
ensemblrs397508528
gopubmedrs397508528
geneviewrs397508528
scholarrs397508528
googlers397508528
pharmgkbrs397508528
gwascentralrs397508528
openSNPrs397508528
23andMers397508528
23andMe allrs397508528
SNP Nexus

SNPshotrs397508528
SNPdbers397508528
MSV3drs397508528
GWAS Ctlgrs397508528
Max Magnitude0
ClinVar
Risk rs397508528(A;A)
Alt rs397508528(A;A)
Reference rs397508528(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171006T>A
CLNSRC ClinVar
CLNACC RCV000046848.2,