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rs397508314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508314(A;C)
Make rs397508314(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592026
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508314
ebirs397508314
HLIrs397508314
Exacrs397508314
Varsomers397508314
Maprs397508314
PheGenIrs397508314
hapmaprs397508314
1000 genomesrs397508314
hgdprs397508314
ensemblrs397508314
gopubmedrs397508314
geneviewrs397508314
scholarrs397508314
googlers397508314
pharmgkbrs397508314
gwascentralrs397508314
openSNPrs397508314
23andMers397508314
23andMe allrs397508314
SNP Nexus

SNPshotrs397508314
SNPdbers397508314
MSV3drs397508314
GWAS Ctlgrs397508314
Max Magnitude0
ClinVar
Risk rs397508314(C,G,T;C,G,T)
Alt rs397508314(C,G,T;C,G,T)
Reference rs397508314(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232080A>C
CLNSRC ClinVar
CLNACC RCV000046496.2,