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rs397508178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508178(C;C)
Make rs397508178(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548640
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508178
ebirs397508178
HLIrs397508178
Exacrs397508178
Varsomers397508178
Maprs397508178
PheGenIrs397508178
hapmaprs397508178
1000 genomesrs397508178
hgdprs397508178
ensemblrs397508178
gopubmedrs397508178
geneviewrs397508178
scholarrs397508178
googlers397508178
pharmgkbrs397508178
gwascentralrs397508178
openSNPrs397508178
23andMers397508178
23andMe allrs397508178
SNP Nexus

SNPshotrs397508178
SNPdbers397508178
MSV3drs397508178
GWAS Ctlgrs397508178
Max Magnitude0
ClinVar
Risk rs397508178(C;C)
Alt rs397508178(C;C)
Reference rs397508178(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188694G>C
CLNSRC ClinVar
CLNACC RCV000046261.2,