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rs757650373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs757650373(-;CGGAGGGAGAGGGAG)
Make rs757650373(CGGAGGGAGAGGGAG;CGGAGGGAGAGGGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position17430884
GeneABCC8
is asnp
is mentioned by
dbSNPrs757650373
ClinGenrs757650373
ebirs757650373
HLIrs757650373
Exacrs757650373
Varsomers757650373
Maprs757650373
PheGenIrs757650373
hapmaprs757650373
1000 genomesrs757650373
hgdprs757650373
ensemblrs757650373
gopubmedrs757650373
geneviewrs757650373
scholarrs757650373
googlers757650373
pharmgkbrs757650373
gwascentralrs757650373
openSNPrs757650373
23andMers757650373
23andMe allrs757650373
SNP Nexus

SNPshotrs757650373
SNPdbers757650373
MSV3drs757650373
GWAS Ctlgrs757650373
Max Magnitude0
ClinVar
Risk rs757650373(GAGGGAGAGGGAGGC;GAGGGAGAGGGAGGC)
Alt rs757650373(GAGGGAGAGGGAGGC;GAGGGAGAGGGAGGC)
Reference Rs757650373(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCC8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.17452432_17452446dupGAGGGAGAGGGAGGC
CLNSRC
CLNACC RCV000201873.1,