rs587777743

Orientation

plus

Stabilized

plus

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

Make rs587777743(A;A)

Make rs587777743(A;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

99557386

Gene

TRMT10A

is a	snp
is	mentioned by
dbSNP	rs587777743
dbSNP (classic)	rs587777743
ClinGen	rs587777743
ebi	rs587777743
HLI	rs587777743
Exac	rs587777743
Gnomad	rs587777743
Varsome	rs587777743
LitVar	rs587777743
Map	rs587777743
PheGenI	rs587777743
Biobank	rs587777743
1000 genomes	rs587777743
hgdp	rs587777743
ensembl	rs587777743
geneview	rs587777743
scholar	rs587777743
google	rs587777743
pharmgkb	rs587777743
gwascentral	rs587777743
openSNP	rs587777743
23andMe	rs587777743
SNPshot	rs587777743
SNPdbe	rs587777743
MSV3d	rs587777743
GWAS Ctlg	rs587777743

Max Magnitude

0

ClinVar
Risk	rs587777743(A;A)
Alt	rs587777743(A;A)
Reference	Rs587777743(G;G)
Significance	Pathogenic
Disease	Microcephaly
Variation	info
Gene	TRMT10A
CLNDBN	Microcephaly, short stature, and impaired glucose metabolism 1
Reversed	0
HGVS	NC_000004.11:g.100478543G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144247.2,