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rs749323139

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749323139(-;-)
Make rs749323139(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position42911150
GeneG6PC
is asnp
is mentioned by
dbSNPrs749323139
dbSNP (classic)rs749323139
ClinGenrs749323139
ebirs749323139
HLIrs749323139
Exacrs749323139
Gnomadrs749323139
Varsomers749323139
LitVarrs749323139
Maprs749323139
PheGenIrs749323139
Biobankrs749323139
1000 genomesrs749323139
hgdprs749323139
ensemblrs749323139
geneviewrs749323139
scholarrs749323139
googlers749323139
pharmgkbrs749323139
gwascentralrs749323139
openSNPrs749323139
23andMers749323139
SNPshotrs749323139
SNPdbers749323139
MSV3drs749323139
GWAS Ctlgrs749323139
Max Magnitude0
ClinVar
Risk rs749323139(-;-)
Alt rs749323139(-;-)
Reference Rs749323139(C;C)
Significance Probable-Pathogenic
Disease Glycogen storage disease type 1A
Variation info
Gene G6PC
CLNDBN Glycogen storage disease type 1A
Reversed 0
HGVS NC_000017.10:g.41063167delC
CLNSRC
CLNACC RCV000411015.1,