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rs397508643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508643(G;T)
Make rs397508643(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652890
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508643
ebirs397508643
HLIrs397508643
Exacrs397508643
Varsomers397508643
Maprs397508643
PheGenIrs397508643
hapmaprs397508643
1000 genomesrs397508643
hgdprs397508643
ensemblrs397508643
gopubmedrs397508643
geneviewrs397508643
scholarrs397508643
googlers397508643
pharmgkbrs397508643
gwascentralrs397508643
openSNPrs397508643
23andMers397508643
23andMe allrs397508643
SNP Nexus

SNPshotrs397508643
SNPdbers397508643
MSV3drs397508643
GWAS Ctlgrs397508643
Max Magnitude0
ClinVar
Risk rs397508643(T;T)
Alt rs397508643(T;T)
Reference rs397508643(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292944G>T
CLNSRC ClinVar
CLNACC RCV000047034.2,