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rs397508512

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508512(G;G)
Make rs397508512(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611617
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508512
ebirs397508512
HLIrs397508512
Exacrs397508512
Varsomers397508512
Maprs397508512
PheGenIrs397508512
hapmaprs397508512
1000 genomesrs397508512
hgdprs397508512
ensemblrs397508512
gopubmedrs397508512
geneviewrs397508512
scholarrs397508512
googlers397508512
pharmgkbrs397508512
gwascentralrs397508512
openSNPrs397508512
23andMers397508512
23andMe allrs397508512
SNP Nexus

SNPshotrs397508512
SNPdbers397508512
MSV3drs397508512
GWAS Ctlgrs397508512
Max Magnitude0
ClinVar
Risk rs397508512(G;G)
Alt rs397508512(G;G)
Reference rs397508512(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251671T>G
CLNSRC ClinVar
CLNACC RCV000046804.2,