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rs387906376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G) 3 cystic fibrosis carrier
(G;G) 0 common in clinvar


Make rs387906376(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592458
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906376
ebirs387906376
HLIrs387906376
Exacrs387906376
Varsomers387906376
Maprs387906376
PheGenIrs387906376
hapmaprs387906376
1000 genomesrs387906376
hgdprs387906376
ensemblrs387906376
gopubmedrs387906376
geneviewrs387906376
scholarrs387906376
googlers387906376
pharmgkbrs387906376
gwascentralrs387906376
openSNPrs387906376
23andMers387906376
23andMe allrs387906376
SNP Nexus

SNPshotrs387906376
SNPdbers387906376
MSV3drs387906376
GWAS Ctlgrs387906376
Max Magnitude3
ClinVar
Risk rs387906376(;)
Alt rs387906376(;)
Reference rs387906376(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232512delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007641.3,