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rs397508145

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508145(-;-)
Make rs397508145(-;G)
Make rs397508145(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540259
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508145
ebirs397508145
HLIrs397508145
Exacrs397508145
Varsomers397508145
Maprs397508145
PheGenIrs397508145
hapmaprs397508145
1000 genomesrs397508145
hgdprs397508145
ensemblrs397508145
gopubmedrs397508145
geneviewrs397508145
scholarrs397508145
googlers397508145
pharmgkbrs397508145
gwascentralrs397508145
openSNPrs397508145
23andMers397508145
23andMe allrs397508145
SNP Nexus

SNPshotrs397508145
SNPdbers397508145
MSV3drs397508145
GWAS Ctlgrs397508145
Max Magnitude0
ClinVar
Risk rs397508145(G;G)
Alt rs397508145(G;G)
Reference rs397508145(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180313_117180314insG
CLNSRC ClinVar
CLNACC RCV000046203.2,