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rs397508366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;T) 3 carrier of a cystic fibrosis allele
Make rs397508366(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509102
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508366
ebirs397508366
HLIrs397508366
Exacrs397508366
Varsomers397508366
Maprs397508366
PheGenIrs397508366
hapmaprs397508366
1000 genomesrs397508366
hgdprs397508366
ensemblrs397508366
gopubmedrs397508366
geneviewrs397508366
scholarrs397508366
googlers397508366
pharmgkbrs397508366
gwascentralrs397508366
openSNPrs397508366
23andMers397508366
23andMe allrs397508366
SNP Nexus

SNPshotrs397508366
SNPdbers397508366
MSV3drs397508366
GWAS Ctlgrs397508366
Max Magnitude3
ClinVar
Risk rs397508366(T;T)
Alt rs397508366(T;T)
Reference rs397508366(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149156dupT
CLNSRC CFTR2
CLNACC RCV000046577.6,