rs886039897

Orientation

plus

Stabilized

plus

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

Make rs886039897(A;A)

Make rs886039897(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

68347630

Gene

PRMT7

is a	snp
is	mentioned by
dbSNP	rs886039897
dbSNP (classic)	rs886039897
ClinGen	rs886039897
ebi	rs886039897
HLI	rs886039897
Exac	rs886039897
Gnomad	rs886039897
Varsome	rs886039897
LitVar	rs886039897
Map	rs886039897
PheGenI	rs886039897
Biobank	rs886039897
1000 genomes	rs886039897
hgdp	rs886039897
ensembl	rs886039897
geneview	rs886039897
scholar	rs886039897
google	rs886039897
pharmgkb	rs886039897
gwascentral	rs886039897
openSNP	rs886039897
23andMe	rs886039897
SNPshot	rs886039897
SNPdbe	rs886039897
MSV3d	rs886039897
GWAS Ctlg	rs886039897

Max Magnitude

0

ClinVar
Risk	rs886039897(A;A)
Alt	rs886039897(A;A)
Reference	Rs886039897(G;G)
Significance	Pathogenic
Disease	Short stature
Variation	info
Gene	PRMT7
CLNDBN	Short stature, brachydactyly, intellectual developmental disability, and seizures
Reversed	0
HGVS	NC_000016.9:g.68381533G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000256479.1,