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rs397508813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397508813(-;-)
Make rs397508813(-;AA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540111
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508813
ebirs397508813
HLIrs397508813
Exacrs397508813
Varsomers397508813
Maprs397508813
PheGenIrs397508813
hapmaprs397508813
1000 genomesrs397508813
hgdprs397508813
ensemblrs397508813
gopubmedrs397508813
geneviewrs397508813
scholarrs397508813
googlers397508813
pharmgkbrs397508813
gwascentralrs397508813
openSNPrs397508813
23andMers397508813
23andMe allrs397508813
SNP Nexus

SNPshotrs397508813
SNPdbers397508813
MSV3drs397508813
GWAS Ctlgrs397508813
Max Magnitude0
ClinVar
Risk rs397508813(;)
Alt rs397508813(;)
Reference rs397508813(AA;AA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180165_117180166delAA
CLNSRC ClinVar
CLNACC RCV000047279.2,