rs1057518850

Orientation

plus

Stabilized

plus

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

Make rs1057518850(A;G)

Make rs1057518850(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

147928320

Gene

FMR1

is a	snp
is	mentioned by
dbSNP	rs1057518850
dbSNP (classic)	rs1057518850
ClinGen	rs1057518850
ebi	rs1057518850
HLI	rs1057518850
Exac	rs1057518850
Gnomad	rs1057518850
Varsome	rs1057518850
LitVar	rs1057518850
Map	rs1057518850
PheGenI	rs1057518850
Biobank	rs1057518850
1000 genomes	rs1057518850
hgdp	rs1057518850
ensembl	rs1057518850
geneview	rs1057518850
scholar	rs1057518850
google	rs1057518850
pharmgkb	rs1057518850
gwascentral	rs1057518850
openSNP	rs1057518850
23andMe	rs1057518850
SNPshot	rs1057518850
SNPdbe	rs1057518850
MSV3d	rs1057518850
GWAS Ctlg	rs1057518850

Max Magnitude

0

ClinVar
Risk	rs1057518850(G;G)
Alt	rs1057518850(G;G)
Reference	Rs1057518850(A;A)
Significance	Probable-Pathogenic
Disease	Autistic behavior Intellectual disability
Variation	info
Gene	FMR1
CLNDBN	Autistic behavior Intellectual disability
Reversed	0
HGVS	NC_000023.10:g.147009838A>G
CLNSRC
CLNACC	RCV000415417.1,