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rs397508377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508377(C;T)
Make rs397508377(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592607
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508377
ebirs397508377
HLIrs397508377
Exacrs397508377
Varsomers397508377
Maprs397508377
PheGenIrs397508377
hapmaprs397508377
1000 genomesrs397508377
hgdprs397508377
ensemblrs397508377
gopubmedrs397508377
geneviewrs397508377
scholarrs397508377
googlers397508377
pharmgkbrs397508377
gwascentralrs397508377
openSNPrs397508377
23andMers397508377
23andMe allrs397508377
SNP Nexus

SNPshotrs397508377
SNPdbers397508377
MSV3drs397508377
GWAS Ctlgrs397508377
Max Magnitude0
ClinVar
Risk rs397508377(T;T)
Alt rs397508377(T;T)
Reference rs397508377(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232661C>T
CLNSRC ClinVar
CLNACC RCV000046593.2,