rs587777014

Orientation

plus

Stabilized

plus

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

Make rs587777014(A;G)

Make rs587777014(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

59152680

Gene

FAM111A

is a	snp
is	mentioned by
dbSNP	rs587777014
dbSNP (classic)	rs587777014
ClinGen	rs587777014
ebi	rs587777014
HLI	rs587777014
Exac	rs587777014
Gnomad	rs587777014
Varsome	rs587777014
LitVar	rs587777014
Map	rs587777014
PheGenI	rs587777014
Biobank	rs587777014
1000 genomes	rs587777014
hgdp	rs587777014
ensembl	rs587777014
geneview	rs587777014
scholar	rs587777014
google	rs587777014
pharmgkb	rs587777014
gwascentral	rs587777014
openSNP	rs587777014
23andMe	rs587777014
SNPshot	rs587777014
SNPdbe	rs587777014
MSV3d	rs587777014
GWAS Ctlg	rs587777014

Max Magnitude

0

ClinVar
Risk	rs587777014(G;G)
Alt	rs587777014(G;G)
Reference	Rs587777014(A;A)
Significance	Other
Disease	Gracile bone dysplasia
Variation	info
Gene	FAM111A
CLNDBN	Gracile bone dysplasia
Reversed	0
HGVS	NC_000011.9:g.58920153A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000050213.4,