rs281875192

Orientation

plus

Stabilized

plus

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

Make rs281875192(C;T)

Make rs281875192(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

2110274

Gene

SMARCA2

is a	snp
is	mentioned by
dbSNP	rs281875192
dbSNP (classic)	rs281875192
ClinGen	rs281875192
ebi	rs281875192
HLI	rs281875192
Exac	rs281875192
Gnomad	rs281875192
Varsome	rs281875192
LitVar	rs281875192
Map	rs281875192
PheGenI	rs281875192
Biobank	rs281875192
1000 genomes	rs281875192
hgdp	rs281875192
ensembl	rs281875192
geneview	rs281875192
scholar	rs281875192
google	rs281875192
pharmgkb	rs281875192
gwascentral	rs281875192
openSNP	rs281875192
23andMe	rs281875192
SNPshot	rs281875192
SNPdbe	rs281875192
MSV3d	rs281875192
GWAS Ctlg	rs281875192

Max Magnitude

0

ClinVar
Risk	rs281875192(G;G) rs281875192(T;T)
Alt	rs281875192(G;G) rs281875192(T;T)
Reference	Rs281875192(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SMARCA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.2110274C>G; NC_000009.11:g.2110274C>T
CLNSRC	UniProtKB (protein) UniProtKB (variants)
CLNACC	RCV000320669.1, RCV000059670.1,