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rs397508360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508360(-;-)
Make rs397508360(-;T)
Make rs397508360(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509096
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508360
ebirs397508360
HLIrs397508360
Exacrs397508360
Varsomers397508360
Maprs397508360
PheGenIrs397508360
hapmaprs397508360
1000 genomesrs397508360
hgdprs397508360
ensemblrs397508360
gopubmedrs397508360
geneviewrs397508360
scholarrs397508360
googlers397508360
pharmgkbrs397508360
gwascentralrs397508360
openSNPrs397508360
23andMers397508360
23andMe allrs397508360
SNP Nexus

SNPshotrs397508360
SNPdbers397508360
MSV3drs397508360
GWAS Ctlgrs397508360
Max Magnitude0
ClinVar
Risk rs397508360(T;T)
Alt rs397508360(T;T)
Reference rs397508360(;)
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,