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rs397508376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508376(-;-)
Make rs397508376(-;T)
Make rs397508376(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592601
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508376
ebirs397508376
HLIrs397508376
Exacrs397508376
Varsomers397508376
Maprs397508376
PheGenIrs397508376
hapmaprs397508376
1000 genomesrs397508376
hgdprs397508376
ensemblrs397508376
gopubmedrs397508376
geneviewrs397508376
scholarrs397508376
googlers397508376
pharmgkbrs397508376
gwascentralrs397508376
openSNPrs397508376
23andMers397508376
23andMe allrs397508376
SNP Nexus

SNPshotrs397508376
SNPdbers397508376
MSV3drs397508376
GWAS Ctlgrs397508376
Max Magnitude0
ClinVar
Risk rs397508376(T;T)
Alt rs397508376(T;T)
Reference rs397508376(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232656dupT
CLNSRC ClinVar
CLNACC RCV000046592.2,