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rs1057519582

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519582(A;A)
Make rs1057519582(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position10874380
GeneGCM2
is asnp
is mentioned by
dbSNPrs1057519582
dbSNP (old)rs1057519582
ClinGenrs1057519582
ebirs1057519582
HLIrs1057519582
Exacrs1057519582
Gnomadrs1057519582
Varsomers1057519582
Maprs1057519582
PheGenIrs1057519582
Biobankrs1057519582
1000 genomesrs1057519582
hgdprs1057519582
ensemblrs1057519582
gopubmedrs1057519582
geneviewrs1057519582
scholarrs1057519582
googlers1057519582
pharmgkbrs1057519582
gwascentralrs1057519582
openSNPrs1057519582
23andMers1057519582
23andMe allrs1057519582
SNPshotrs1057519582
SNPdbers1057519582
MSV3drs1057519582
GWAS Ctlgrs1057519582
Max Magnitude0
ClinVar
Risk rs1057519582(A;A)
Alt rs1057519582(A;A)
Reference Rs1057519582(T;T)
Significance Pathogenic
Disease Hyperparathyroidism 4
Variation info
Gene GCM2
CLNDBN Hyperparathyroidism 4
Reversed 1
HGVS NC_000006.11:g.10874613A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000417072.1,