rs797044856

Orientation

plus

Stabilized

plus

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

Make rs797044856(C;C)

Make rs797044856(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

11021968

Gene

SMARCA4

is a	snp
is	mentioned by
dbSNP	rs797044856
dbSNP (classic)	rs797044856
ClinGen	rs797044856
ebi	rs797044856
HLI	rs797044856
Exac	rs797044856
Gnomad	rs797044856
Varsome	rs797044856
LitVar	rs797044856
Map	rs797044856
PheGenI	rs797044856
Biobank	rs797044856
1000 genomes	rs797044856
hgdp	rs797044856
ensembl	rs797044856
geneview	rs797044856
scholar	rs797044856
google	rs797044856
pharmgkb	rs797044856
gwascentral	rs797044856
openSNP	rs797044856
23andMe	rs797044856
SNPshot	rs797044856
SNPdbe	rs797044856
MSV3d	rs797044856
GWAS Ctlg	rs797044856

Max Magnitude

0

ClinVar
Risk	rs797044856(C;C)
Alt	rs797044856(C;C)
Reference	Rs797044856(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	SMARCA4
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000019.9:g.11132644G>C
CLNSRC
CLNACC	RCV000190658.1,