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rs397508587

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 3 Carrier for a cystic fibrosis allele
(A;A) 0 common in clinvar


Make rs397508587(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627658
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508587
ebirs397508587
HLIrs397508587
Exacrs397508587
Varsomers397508587
Maprs397508587
PheGenIrs397508587
hapmaprs397508587
1000 genomesrs397508587
hgdprs397508587
ensemblrs397508587
gopubmedrs397508587
geneviewrs397508587
scholarrs397508587
googlers397508587
pharmgkbrs397508587
gwascentralrs397508587
openSNPrs397508587
23andMers397508587
23andMe allrs397508587
SNP Nexus

SNPshotrs397508587
SNPdbers397508587
MSV3drs397508587
GWAS Ctlgrs397508587
Max Magnitude3

Cystic fibrosis; c.3605delA, p.Asp1202Alafs

named i5011956 by 23andMe

ClinVar
Risk rs397508587(;)
Alt rs397508587(;)
Reference rs397508587(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267712delA
CLNSRC CFTR2
CLNACC RCV000046933.3,