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rs397508604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 3 carrier of a cystic fibrosis allele
(T;T) 0 common in clinvar


Make rs397508604(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642481
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508604
ebirs397508604
HLIrs397508604
Exacrs397508604
Varsomers397508604
Maprs397508604
PheGenIrs397508604
hapmaprs397508604
1000 genomesrs397508604
hgdprs397508604
ensemblrs397508604
gopubmedrs397508604
geneviewrs397508604
scholarrs397508604
googlers397508604
pharmgkbrs397508604
gwascentralrs397508604
openSNPrs397508604
23andMers397508604
23andMe allrs397508604
SNP Nexus

SNPshotrs397508604
SNPdbers397508604
MSV3drs397508604
GWAS Ctlgrs397508604
Max Magnitude3
ClinVar
Risk rs397508604(G;G)
Alt rs397508604(G;G)
Reference rs397508604(T;T)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282535T>G
CLNSRC CFTR2
CLNACC RCV000046973.3,