rs1057519582

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs1057519582(A;A)

Make rs1057519582(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

10874380

Gene

GCM2

is a	snp
is	mentioned by
dbSNP	rs1057519582
dbSNP (classic)	rs1057519582
ClinGen	rs1057519582
ebi	rs1057519582
HLI	rs1057519582
Exac	rs1057519582
Gnomad	rs1057519582
Varsome	rs1057519582
LitVar	rs1057519582
Map	rs1057519582
PheGenI	rs1057519582
Biobank	rs1057519582
1000 genomes	rs1057519582
hgdp	rs1057519582
ensembl	rs1057519582
geneview	rs1057519582
scholar	rs1057519582
google	rs1057519582
pharmgkb	rs1057519582
gwascentral	rs1057519582
openSNP	rs1057519582
23andMe	rs1057519582
SNPshot	rs1057519582
SNPdbe	rs1057519582
MSV3d	rs1057519582
GWAS Ctlg	rs1057519582

Max Magnitude

0

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,