rs3734354

Orientation

minus

Stabilized

minus

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

Make rs3734354(A;A)

Make rs3734354(A;C)

Reference

GRCh38 38.1/141

Chromosome

6

Position

100420903

Gene	LOC102724406, SIM1

is a	snp
is	mentioned by
dbSNP	rs3734354
dbSNP (classic)	rs3734354
ClinGen	rs3734354
ebi	rs3734354
HLI	rs3734354
Exac	rs3734354
Gnomad	rs3734354
Varsome	rs3734354
LitVar	rs3734354
Map	rs3734354
PheGenI	rs3734354
Biobank	rs3734354
1000 genomes	rs3734354
hgdp	rs3734354
ensembl	rs3734354
geneview	rs3734354
scholar	rs3734354
google	rs3734354
pharmgkb	rs3734354
gwascentral	rs3734354
openSNP	rs3734354
23andMe	rs3734354
SNPshot	rs3734354
SNPdbe	rs3734354
MSV3d	rs3734354
GWAS Ctlg	rs3734354

GMAF

0.197

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 20075856] Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population

[PMID 21512513] Replication and extension of association between common genetic variants in SIM1 and human adiposity

[PMID 17357083] Medical sequencing at the extremes of human body mass.

[PMID 19401419] Common variation in SIM1 is reproducibly associated with BMI in Pima Indians.

[PMID 21671989] Dosing equation for tacrolimus using genetic variants and clinical factors.

ClinVar
Risk	rs3734354(A;A) rs3734354(T;T)
Alt	rs3734354(A;A) rs3734354(T;T)
Reference	Rs3734354(C;C)
Significance	Non-pathogenic
Disease	Schaaf-yang syndrome
Variation	info
Gene	SIM1
CLNDBN	Schaaf-yang syndrome
Reversed	1
HGVS	NC_000006.11:g.100868779G>T
CLNSRC
CLNACC	RCV000405629.1,