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rs397508578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508578(A;T)
Make rs397508578(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627582
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508578
ebirs397508578
HLIrs397508578
Exacrs397508578
Varsomers397508578
Maprs397508578
PheGenIrs397508578
hapmaprs397508578
1000 genomesrs397508578
hgdprs397508578
ensemblrs397508578
gopubmedrs397508578
geneviewrs397508578
scholarrs397508578
googlers397508578
pharmgkbrs397508578
gwascentralrs397508578
openSNPrs397508578
23andMers397508578
23andMe allrs397508578
SNP Nexus

SNPshotrs397508578
SNPdbers397508578
MSV3drs397508578
GWAS Ctlgrs397508578
Max Magnitude0
ClinVar
Risk rs397508578(T;T)
Alt rs397508578(T;T)
Reference rs397508578(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267636A>T
CLNSRC ClinVar
CLNACC RCV000046921.2,