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rs397508184

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAAAA;CAAAA) 0 common in clinvar
Make rs397508184(-;-)
Make rs397508184(-;CAAAA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548671
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508184
ebirs397508184
HLIrs397508184
Exacrs397508184
Varsomers397508184
Maprs397508184
PheGenIrs397508184
hapmaprs397508184
1000 genomesrs397508184
hgdprs397508184
ensemblrs397508184
gopubmedrs397508184
geneviewrs397508184
scholarrs397508184
googlers397508184
pharmgkbrs397508184
gwascentralrs397508184
openSNPrs397508184
23andMers397508184
23andMe allrs397508184
SNP Nexus

SNPshotrs397508184
SNPdbers397508184
MSV3drs397508184
GWAS Ctlgrs397508184
Max Magnitude0
ClinVar
Risk rs397508184(;)
Alt rs397508184(;)
Reference rs397508184(CAAAA;CAAAA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188725_117188729delCAAAA
CLNSRC ClinVar
CLNACC RCV000046267.2,