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rs397508504

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508504(C;C)
Make rs397508504(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610669
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508504
ebirs397508504
HLIrs397508504
Exacrs397508504
Varsomers397508504
Maprs397508504
PheGenIrs397508504
hapmaprs397508504
1000 genomesrs397508504
hgdprs397508504
ensemblrs397508504
gopubmedrs397508504
geneviewrs397508504
scholarrs397508504
googlers397508504
pharmgkbrs397508504
gwascentralrs397508504
openSNPrs397508504
23andMers397508504
23andMe allrs397508504
SNP Nexus

SNPshotrs397508504
SNPdbers397508504
MSV3drs397508504
GWAS Ctlgrs397508504
Max Magnitude0
ClinVar
Risk rs397508504(C;C)
Alt rs397508504(C;C)
Reference rs397508504(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250723G>C
CLNSRC ClinVar
CLNACC RCV000046790.2,