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rs397508514

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508514(A;A)
Make rs397508514(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611630
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508514
ebirs397508514
HLIrs397508514
Exacrs397508514
Varsomers397508514
Maprs397508514
PheGenIrs397508514
hapmaprs397508514
1000 genomesrs397508514
hgdprs397508514
ensemblrs397508514
gopubmedrs397508514
geneviewrs397508514
scholarrs397508514
googlers397508514
pharmgkbrs397508514
gwascentralrs397508514
openSNPrs397508514
23andMers397508514
23andMe allrs397508514
SNP Nexus

SNPshotrs397508514
SNPdbers397508514
MSV3drs397508514
GWAS Ctlgrs397508514
Max Magnitude0
ClinVar
Risk rs397508514(A;A)
Alt rs397508514(A;A)
Reference rs397508514(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251684G>A
CLNSRC ClinVar
CLNACC RCV000046809.2,