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rs397508252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508252(-;-)
Make rs397508252(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587806
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508252
ebirs397508252
HLIrs397508252
Exacrs397508252
Varsomers397508252
Maprs397508252
PheGenIrs397508252
hapmaprs397508252
1000 genomesrs397508252
hgdprs397508252
ensemblrs397508252
gopubmedrs397508252
geneviewrs397508252
scholarrs397508252
googlers397508252
pharmgkbrs397508252
gwascentralrs397508252
openSNPrs397508252
23andMers397508252
23andMe allrs397508252
SNP Nexus

SNPshotrs397508252
SNPdbers397508252
MSV3drs397508252
GWAS Ctlgrs397508252
Max Magnitude0
ClinVar
Risk rs397508252(;)
Alt rs397508252(;)
Reference rs397508252(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227860delG
CLNSRC ClinVar
CLNACC RCV000046390.2,