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rs397508529

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508529(-;-)
Make rs397508529(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611728
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508529
ebirs397508529
HLIrs397508529
Exacrs397508529
Varsomers397508529
Maprs397508529
PheGenIrs397508529
hapmaprs397508529
1000 genomesrs397508529
hgdprs397508529
ensemblrs397508529
gopubmedrs397508529
geneviewrs397508529
scholarrs397508529
googlers397508529
pharmgkbrs397508529
gwascentralrs397508529
openSNPrs397508529
23andMers397508529
23andMe allrs397508529
SNP Nexus

SNPshotrs397508529
SNPdbers397508529
MSV3drs397508529
GWAS Ctlgrs397508529
Max Magnitude0
ClinVar
Risk rs397508529(;)
Alt rs397508529(;)
Reference rs397508529(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251782delT
CLNSRC ClinVar
CLNACC RCV000046850.2,