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rs397508146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508146(C;C)
Make rs397508146(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540267
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508146
ebirs397508146
HLIrs397508146
Exacrs397508146
Varsomers397508146
Maprs397508146
PheGenIrs397508146
hapmaprs397508146
1000 genomesrs397508146
hgdprs397508146
ensemblrs397508146
gopubmedrs397508146
geneviewrs397508146
scholarrs397508146
googlers397508146
pharmgkbrs397508146
gwascentralrs397508146
openSNPrs397508146
23andMers397508146
23andMe allrs397508146
SNP Nexus

SNPshotrs397508146
SNPdbers397508146
MSV3drs397508146
GWAS Ctlgrs397508146
Max Magnitude0
ClinVar
Risk rs397508146(C;C)
Alt rs397508146(C;C)
Reference rs397508146(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180321T>C
CLNSRC ClinVar
CLNACC RCV000046205.2,