rs587777011

Orientation

plus

Stabilized

plus

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

Make rs587777011(A;A)

Make rs587777011(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

59153374

Gene

FAM111A

is a	snp
is	mentioned by
dbSNP	rs587777011
dbSNP (classic)	rs587777011
ClinGen	rs587777011
ebi	rs587777011
HLI	rs587777011
Exac	rs587777011
Gnomad	rs587777011
Varsome	rs587777011
LitVar	rs587777011
Map	rs587777011
PheGenI	rs587777011
Biobank	rs587777011
1000 genomes	rs587777011
hgdp	rs587777011
ensembl	rs587777011
geneview	rs587777011
scholar	rs587777011
google	rs587777011
pharmgkb	rs587777011
gwascentral	rs587777011
openSNP	rs587777011
23andMe	rs587777011
SNPshot	rs587777011
SNPdbe	rs587777011
MSV3d	rs587777011
GWAS Ctlg	rs587777011

Max Magnitude

0

ClinVar
Risk	rs587777011(A;A)
Alt	rs587777011(A;A)
Reference	Rs587777011(G;G)
Significance	Other
Disease	Kenny-Caffey syndrome type 2 not provided
Variation	info
Gene	FAM111A
CLNDBN	Kenny-Caffey syndrome type 2 not provided
Reversed	0
HGVS	NC_000011.9:g.58920847G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000050209.4, RCV000419087.1,