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rs1057519581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519581(C;G)
Make rs1057519581(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position10874765
GeneGCM2
is asnp
is mentioned by
dbSNPrs1057519581
dbSNP (old)rs1057519581
ClinGenrs1057519581
ebirs1057519581
HLIrs1057519581
Exacrs1057519581
Gnomadrs1057519581
Varsomers1057519581
Maprs1057519581
PheGenIrs1057519581
Biobankrs1057519581
1000 genomesrs1057519581
hgdprs1057519581
ensemblrs1057519581
gopubmedrs1057519581
geneviewrs1057519581
scholarrs1057519581
googlers1057519581
pharmgkbrs1057519581
gwascentralrs1057519581
openSNPrs1057519581
23andMers1057519581
23andMe allrs1057519581
SNPshotrs1057519581
SNPdbers1057519581
MSV3drs1057519581
GWAS Ctlgrs1057519581
Max Magnitude0
ClinVar
Risk rs1057519581(G;G)
Alt rs1057519581(G;G)
Reference Rs1057519581(C;C)
Significance Pathogenic
Disease Hyperparathyroidism 4
Variation info
Gene GCM2
CLNDBN Hyperparathyroidism 4
Reversed 1
HGVS NC_000006.11:g.10874998G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000417072.1,