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rs397508780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508780(C;C)
Make rs397508780(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535341
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508780
ebirs397508780
HLIrs397508780
Exacrs397508780
Varsomers397508780
Maprs397508780
PheGenIrs397508780
hapmaprs397508780
1000 genomesrs397508780
hgdprs397508780
ensemblrs397508780
gopubmedrs397508780
geneviewrs397508780
scholarrs397508780
googlers397508780
pharmgkbrs397508780
gwascentralrs397508780
openSNPrs397508780
23andMers397508780
23andMe allrs397508780
SNP Nexus

SNPshotrs397508780
SNPdbers397508780
MSV3drs397508780
GWAS Ctlgrs397508780
Max Magnitude0
ClinVar
Risk rs397508780(C;C)
Alt rs397508780(C;C)
Reference rs397508780(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175395T>C
CLNSRC ClinVar
CLNACC RCV000047232.2,