rs1057518333

Orientation

minus

Stabilized

minus

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

Make rs1057518333(A;A)

Make rs1057518333(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

100393759

Gene	LOC102724406, SIM1

is a	snp
is	mentioned by
dbSNP	rs1057518333
dbSNP (classic)	rs1057518333
ClinGen	rs1057518333
ebi	rs1057518333
HLI	rs1057518333
Exac	rs1057518333
Gnomad	rs1057518333
Varsome	rs1057518333
LitVar	rs1057518333
Map	rs1057518333
PheGenI	rs1057518333
Biobank	rs1057518333
1000 genomes	rs1057518333
hgdp	rs1057518333
ensembl	rs1057518333
geneview	rs1057518333
scholar	rs1057518333
google	rs1057518333
pharmgkb	rs1057518333
gwascentral	rs1057518333
openSNP	rs1057518333
23andMe	rs1057518333
SNPshot	rs1057518333
SNPdbe	rs1057518333
MSV3d	rs1057518333
GWAS Ctlg	rs1057518333

Max Magnitude

0

ClinVar
Risk	rs1057518333(A;A)
Alt	rs1057518333(A;A)
Reference	Rs1057518333(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SIM1
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.100841635G>T
CLNSRC
CLNACC	RCV000414358.1,