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rs397508190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397508190(-;-)
Make rs397508190(-;AT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548761
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508190
ebirs397508190
HLIrs397508190
Exacrs397508190
Varsomers397508190
Maprs397508190
PheGenIrs397508190
hapmaprs397508190
1000 genomesrs397508190
hgdprs397508190
ensemblrs397508190
gopubmedrs397508190
geneviewrs397508190
scholarrs397508190
googlers397508190
pharmgkbrs397508190
gwascentralrs397508190
openSNPrs397508190
23andMers397508190
23andMe allrs397508190
SNP Nexus

SNPshotrs397508190
SNPdbers397508190
MSV3drs397508190
GWAS Ctlgrs397508190
Max Magnitude0
ClinVar
Risk rs397508190(;)
Alt rs397508190(;)
Reference rs397508190(AT;AT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188815_117188816delAT
CLNSRC ClinVar
CLNACC RCV000046276.2,