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rs397508615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508615(C;T)
Make rs397508615(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642561
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508615
ebirs397508615
HLIrs397508615
Exacrs397508615
Varsomers397508615
Maprs397508615
PheGenIrs397508615
hapmaprs397508615
1000 genomesrs397508615
hgdprs397508615
ensemblrs397508615
gopubmedrs397508615
geneviewrs397508615
scholarrs397508615
googlers397508615
pharmgkbrs397508615
gwascentralrs397508615
openSNPrs397508615
23andMers397508615
23andMe allrs397508615
SNP Nexus

SNPshotrs397508615
SNPdbers397508615
MSV3drs397508615
GWAS Ctlgrs397508615
Max Magnitude0
ClinVar
Risk rs397508615(G,T;G,T)
Alt rs397508615(G,T;G,T)
Reference rs397508615(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282615C>T
CLNSRC ClinVar
CLNACC RCV000046991.2,