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rs397508334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508334(-;-)
Make rs397508334(-;C)
Make rs397508334(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592211
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508334
ebirs397508334
HLIrs397508334
Exacrs397508334
Varsomers397508334
Maprs397508334
PheGenIrs397508334
hapmaprs397508334
1000 genomesrs397508334
hgdprs397508334
ensemblrs397508334
gopubmedrs397508334
geneviewrs397508334
scholarrs397508334
googlers397508334
pharmgkbrs397508334
gwascentralrs397508334
openSNPrs397508334
23andMers397508334
23andMe allrs397508334
SNP Nexus

SNPshotrs397508334
SNPdbers397508334
MSV3drs397508334
GWAS Ctlgrs397508334
Max Magnitude0
ClinVar
Risk rs397508334(C;C)
Alt rs397508334(C;C)
Reference rs397508334(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232266dupC
CLNSRC ClinVar
CLNACC RCV000046526.2,