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rs397508355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGATACTG;CGATACTG) 0 common in clinvar
(GCGATACT;GCGATACT) 0 common in clinvar
Make rs397508355(-;-)
Make rs397508355(-;CGATACTG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592407
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508355
ebirs397508355
HLIrs397508355
Exacrs397508355
Varsomers397508355
Maprs397508355
PheGenIrs397508355
hapmaprs397508355
1000 genomesrs397508355
hgdprs397508355
ensemblrs397508355
gopubmedrs397508355
geneviewrs397508355
scholarrs397508355
googlers397508355
pharmgkbrs397508355
gwascentralrs397508355
openSNPrs397508355
23andMers397508355
23andMe allrs397508355
SNP Nexus

SNPshotrs397508355
SNPdbers397508355
MSV3drs397508355
GWAS Ctlgrs397508355
Max Magnitude0
ClinVar
Risk rs397508355(;)
Alt rs397508355(;)
Reference rs397508355(GCGATACT;GCGATACT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232461_117232468delCGATACTG
CLNSRC ClinVar
CLNACC RCV000046559.2,