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rs397508362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508362(-;-)
Make rs397508362(-;T)
Make rs397508362(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509097
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508362
ebirs397508362
HLIrs397508362
Exacrs397508362
Varsomers397508362
Maprs397508362
PheGenIrs397508362
hapmaprs397508362
1000 genomesrs397508362
hgdprs397508362
ensemblrs397508362
gopubmedrs397508362
geneviewrs397508362
scholarrs397508362
googlers397508362
pharmgkbrs397508362
gwascentralrs397508362
openSNPrs397508362
23andMers397508362
23andMe allrs397508362
SNP Nexus

SNPshotrs397508362
SNPdbers397508362
MSV3drs397508362
GWAS Ctlgrs397508362
Max Magnitude0
ClinVar
Risk rs397508362(T;T)
Alt rs397508362(T;T)
Reference rs397508362(;)
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,