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rs397508575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs397508575(-;-)
Make rs397508575(-;GA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627538
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508575
ebirs397508575
HLIrs397508575
Exacrs397508575
Varsomers397508575
Maprs397508575
PheGenIrs397508575
hapmaprs397508575
1000 genomesrs397508575
hgdprs397508575
ensemblrs397508575
gopubmedrs397508575
geneviewrs397508575
scholarrs397508575
googlers397508575
pharmgkbrs397508575
gwascentralrs397508575
openSNPrs397508575
23andMers397508575
23andMe allrs397508575
SNP Nexus

SNPshotrs397508575
SNPdbers397508575
MSV3drs397508575
GWAS Ctlgrs397508575
Max Magnitude0
ClinVar
Risk rs397508575(;)
Alt rs397508575(;)
Reference rs397508575(GA;GA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267592_117267593delGA
CLNSRC ClinVar
CLNACC RCV000046911.2,