rs797044959

Orientation

plus

Stabilized

plus

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

Make rs797044959(A;A)

Make rs797044959(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

73914836

Gene

ACTG2

is a	snp
is	mentioned by
dbSNP	rs797044959
dbSNP (classic)	rs797044959
ClinGen	rs797044959
ebi	rs797044959
HLI	rs797044959
Exac	rs797044959
Gnomad	rs797044959
Varsome	rs797044959
LitVar	rs797044959
Map	rs797044959
PheGenI	rs797044959
Biobank	rs797044959
1000 genomes	rs797044959
hgdp	rs797044959
ensembl	rs797044959
geneview	rs797044959
scholar	rs797044959
google	rs797044959
pharmgkb	rs797044959
gwascentral	rs797044959
openSNP	rs797044959
23andMe	rs797044959
SNPshot	rs797044959
SNPdbe	rs797044959
MSV3d	rs797044959
GWAS Ctlg	rs797044959

Max Magnitude

0

ClinVar
Risk	rs797044959(A;A)
Alt	rs797044959(A;A)
Reference	Rs797044959(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases Chronic intestinal pseudoobstruction Megacystis
Variation	info
Gene	ACTG2
CLNDBN	Inborn genetic diseases Chronic intestinal pseudoobstruction Megacystis
Reversed	0
HGVS	NC_000002.11:g.74141963G>A
CLNSRC
CLNACC	RCV000190820.1, RCV000210360.1,