Have questions? Visit https://www.reddit.com/r/SNPedia

rs886039897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039897(A;A)
Make rs886039897(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position68347630
GenePRMT7
is asnp
is mentioned by
dbSNPrs886039897
dbSNP (classic)rs886039897
ClinGenrs886039897
ebirs886039897
HLIrs886039897
Exacrs886039897
Gnomadrs886039897
Varsomers886039897
LitVarrs886039897
Maprs886039897
PheGenIrs886039897
Biobankrs886039897
1000 genomesrs886039897
hgdprs886039897
ensemblrs886039897
geneviewrs886039897
scholarrs886039897
googlers886039897
pharmgkbrs886039897
gwascentralrs886039897
openSNPrs886039897
23andMers886039897
23andMe allrs886039897
SNPshotrs886039897
SNPdbers886039897
MSV3drs886039897
GWAS Ctlgrs886039897
Max Magnitude0
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,