rs1057518038

Orientation

plus

Stabilized

plus

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

Make rs1057518038(A;G)

Make rs1057518038(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

147940643

Gene

FMR1

is a	snp
is	mentioned by
dbSNP	rs1057518038
dbSNP (classic)	rs1057518038
ClinGen	rs1057518038
ebi	rs1057518038
HLI	rs1057518038
Exac	rs1057518038
Gnomad	rs1057518038
Varsome	rs1057518038
LitVar	rs1057518038
Map	rs1057518038
PheGenI	rs1057518038
Biobank	rs1057518038
1000 genomes	rs1057518038
hgdp	rs1057518038
ensembl	rs1057518038
geneview	rs1057518038
scholar	rs1057518038
google	rs1057518038
pharmgkb	rs1057518038
gwascentral	rs1057518038
openSNP	rs1057518038
23andMe	rs1057518038
SNPshot	rs1057518038
SNPdbe	rs1057518038
MSV3d	rs1057518038
GWAS Ctlg	rs1057518038

Max Magnitude

0

ClinVar
Risk	rs1057518038(G;G)
Alt	rs1057518038(G;G)
Reference	Rs1057518038(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FMR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.147022162A>G
CLNSRC
CLNACC	RCV000413972.1,