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rs397508379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508379(G;T)
Make rs397508379(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592634
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508379
ebirs397508379
HLIrs397508379
Exacrs397508379
Varsomers397508379
Maprs397508379
PheGenIrs397508379
hapmaprs397508379
1000 genomesrs397508379
hgdprs397508379
ensemblrs397508379
gopubmedrs397508379
geneviewrs397508379
scholarrs397508379
googlers397508379
pharmgkbrs397508379
gwascentralrs397508379
openSNPrs397508379
23andMers397508379
23andMe allrs397508379
SNP Nexus

SNPshotrs397508379
SNPdbers397508379
MSV3drs397508379
GWAS Ctlgrs397508379
Max Magnitude0
ClinVar
Risk rs397508379(T;T)
Alt rs397508379(T;T)
Reference rs397508379(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232688G>T
CLNSRC ClinVar
CLNACC RCV000046596.2,