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rs397508339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508339(-;-)
Make rs397508339(-;G)
Make rs397508339(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592250
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508339
ebirs397508339
HLIrs397508339
Exacrs397508339
Varsomers397508339
Maprs397508339
PheGenIrs397508339
hapmaprs397508339
1000 genomesrs397508339
hgdprs397508339
ensemblrs397508339
gopubmedrs397508339
geneviewrs397508339
scholarrs397508339
googlers397508339
pharmgkbrs397508339
gwascentralrs397508339
openSNPrs397508339
23andMers397508339
23andMe allrs397508339
SNP Nexus

SNPshotrs397508339
SNPdbers397508339
MSV3drs397508339
GWAS Ctlgrs397508339
Max Magnitude0
ClinVar
Risk rs397508339(G;G)
Alt rs397508339(G;G)
Reference rs397508339(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232304dupG
CLNSRC ClinVar
CLNACC RCV000046535.2,