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rs397508576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508576(-;-)
Make rs397508576(-;T)
Make rs397508576(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627543
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508576
ebirs397508576
HLIrs397508576
Exacrs397508576
Varsomers397508576
Maprs397508576
PheGenIrs397508576
hapmaprs397508576
1000 genomesrs397508576
hgdprs397508576
ensemblrs397508576
gopubmedrs397508576
geneviewrs397508576
scholarrs397508576
googlers397508576
pharmgkbrs397508576
gwascentralrs397508576
openSNPrs397508576
23andMers397508576
23andMe allrs397508576
SNP Nexus

SNPshotrs397508576
SNPdbers397508576
MSV3drs397508576
GWAS Ctlgrs397508576
Max Magnitude0
ClinVar
Risk rs397508576(T;T)
Alt rs397508576(T;T)
Reference rs397508576(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267599dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007652.3,