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rs397508380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508380(-;-)
Make rs397508380(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592639
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508380
ebirs397508380
HLIrs397508380
Exacrs397508380
Varsomers397508380
Maprs397508380
PheGenIrs397508380
hapmaprs397508380
1000 genomesrs397508380
hgdprs397508380
ensemblrs397508380
gopubmedrs397508380
geneviewrs397508380
scholarrs397508380
googlers397508380
pharmgkbrs397508380
gwascentralrs397508380
openSNPrs397508380
23andMers397508380
23andMe allrs397508380
SNP Nexus

SNPshotrs397508380
SNPdbers397508380
MSV3drs397508380
GWAS Ctlgrs397508380
Max Magnitude0
ClinVar
Risk rs397508380(;)
Alt rs397508380(;)
Reference rs397508380(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232693delT
CLNSRC ClinVar
CLNACC RCV000046597.2,