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rs397508526

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs397508526(-;-)
Make rs397508526(-;AT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530951
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508526
ebirs397508526
HLIrs397508526
Exacrs397508526
Varsomers397508526
Maprs397508526
PheGenIrs397508526
hapmaprs397508526
1000 genomesrs397508526
hgdprs397508526
ensemblrs397508526
gopubmedrs397508526
geneviewrs397508526
scholarrs397508526
googlers397508526
pharmgkbrs397508526
gwascentralrs397508526
openSNPrs397508526
23andMers397508526
23andMe allrs397508526
SNP Nexus

SNPshotrs397508526
SNPdbers397508526
MSV3drs397508526
GWAS Ctlgrs397508526
Max Magnitude0
ClinVar
Risk rs397508526(;)
Alt rs397508526(;)
Reference rs397508526(TA;TA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171005_117171006delAT
CLNSRC ClinVar
CLNACC RCV000046844.2,