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rs387906362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 carrier of a cystic fibrosis allele
Make rs387906362(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627774
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906362
ebirs387906362
HLIrs387906362
Exacrs387906362
Varsomers387906362
Maprs387906362
PheGenIrs387906362
hapmaprs387906362
1000 genomesrs387906362
hgdprs387906362
ensemblrs387906362
gopubmedrs387906362
geneviewrs387906362
scholarrs387906362
googlers387906362
pharmgkbrs387906362
gwascentralrs387906362
openSNPrs387906362
23andMers387906362
23andMe allrs387906362
SNP Nexus

SNPshotrs387906362
SNPdbers387906362
MSV3drs387906362
GWAS Ctlgrs387906362
Max Magnitude3
ClinVar
Risk rs387906362(G;G)
Alt rs387906362(G;G)
Reference rs387906362(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267828A>G
CLNSRC CFTR2 Cystic Fibrosis Mutation Database OMIM Allelic Variant
CLNACC RCV000007558.3,