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rs397508246

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397508246(-;-)
Make rs397508246(-;CT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587796
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508246
ebirs397508246
HLIrs397508246
Exacrs397508246
Varsomers397508246
Maprs397508246
PheGenIrs397508246
hapmaprs397508246
1000 genomesrs397508246
hgdprs397508246
ensemblrs397508246
gopubmedrs397508246
geneviewrs397508246
scholarrs397508246
googlers397508246
pharmgkbrs397508246
gwascentralrs397508246
openSNPrs397508246
23andMers397508246
23andMe allrs397508246
SNP Nexus

SNPshotrs397508246
SNPdbers397508246
MSV3drs397508246
GWAS Ctlgrs397508246
Max Magnitude0
ClinVar
Risk rs397508246(;)
Alt rs397508246(;)
Reference rs397508246(CT;CT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227850_117227851delCT
CLNSRC ClinVar
CLNACC RCV000046374.2,