rs587777707

Orientation

plus

Stabilized

plus

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

Make rs587777707(G;T)

Make rs587777707(T;T)

Reference

GRCh38 38.1/142

Chromosome

19

Position

3110191

Gene

GNA11

is a	snp
is	mentioned by
dbSNP	rs587777707
dbSNP (classic)	rs587777707
ClinGen	rs587777707
ebi	rs587777707
HLI	rs587777707
Exac	rs587777707
Gnomad	rs587777707
Varsome	rs587777707
LitVar	rs587777707
Map	rs587777707
PheGenI	rs587777707
Biobank	rs587777707
1000 genomes	rs587777707
hgdp	rs587777707
ensembl	rs587777707
geneview	rs587777707
scholar	rs587777707
google	rs587777707
pharmgkb	rs587777707
gwascentral	rs587777707
openSNP	rs587777707
23andMe	rs587777707
SNPshot	rs587777707
SNPdbe	rs587777707
MSV3d	rs587777707
GWAS Ctlg	rs587777707

Max Magnitude

0

ClinVar
Risk	rs587777707(T;T)
Alt	rs587777707(T;T)
Reference	Rs587777707(G;G)
Significance	Pathogenic
Disease	Hypocalcemia
Variation	info
Gene	GNA11
CLNDBN	Hypocalcemia, autosomal dominant 2
Reversed	0
HGVS	NC_000019.9:g.3110189G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144048.2,