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rs397508696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508696(A;A)
Make rs397508696(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665523
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508696
ebirs397508696
HLIrs397508696
Exacrs397508696
Varsomers397508696
Maprs397508696
PheGenIrs397508696
hapmaprs397508696
1000 genomesrs397508696
hgdprs397508696
ensemblrs397508696
gopubmedrs397508696
geneviewrs397508696
scholarrs397508696
googlers397508696
pharmgkbrs397508696
gwascentralrs397508696
openSNPrs397508696
23andMers397508696
23andMe allrs397508696
SNP Nexus

SNPshotrs397508696
SNPdbers397508696
MSV3drs397508696
GWAS Ctlgrs397508696
Max Magnitude0
ClinVar
Risk rs397508696(A,T;A,T)
Alt rs397508696(A,T;A,T)
Reference rs397508696(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305577G>A; NC_000007.13:g.117305577G>T
CLNSRC ClinVar
CLNACC RCV000047103.2, RCV000047104.2,