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rs397508315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508315(G;G)
Make rs397508315(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592027
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508315
ebirs397508315
HLIrs397508315
Exacrs397508315
Varsomers397508315
Maprs397508315
PheGenIrs397508315
hapmaprs397508315
1000 genomesrs397508315
hgdprs397508315
ensemblrs397508315
gopubmedrs397508315
geneviewrs397508315
scholarrs397508315
googlers397508315
pharmgkbrs397508315
gwascentralrs397508315
openSNPrs397508315
23andMers397508315
23andMe allrs397508315
SNP Nexus

SNPshotrs397508315
SNPdbers397508315
MSV3drs397508315
GWAS Ctlgrs397508315
Max Magnitude0
ClinVar
Risk rs397508315(G;G)
Alt rs397508315(G;G)
Reference rs397508315(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232081T>G
CLNSRC ClinVar
CLNACC RCV000046497.2,