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rs397508628

From SNPedia

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


Make rs397508628(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652850
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508628
ebirs397508628
HLIrs397508628
Exacrs397508628
Varsomers397508628
Maprs397508628
PheGenIrs397508628
hapmaprs397508628
1000 genomesrs397508628
hgdprs397508628
ensemblrs397508628
gopubmedrs397508628
geneviewrs397508628
scholarrs397508628
googlers397508628
pharmgkbrs397508628
gwascentralrs397508628
openSNPrs397508628
23andMers397508628
23andMe allrs397508628
SNP Nexus

SNPshotrs397508628
SNPdbers397508628
MSV3drs397508628
GWAS Ctlgrs397508628
Max Magnitude3
ClinVar
Risk rs397508628(;)
Alt rs397508628(;)
Reference rs397508628(TATT;TATT)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292905_117292908delATTT
CLNSRC CFTR2 OMIM Allelic Variant
CLNACC RCV000047015.5,