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

rs387906986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906986(A;G)
Make rs387906986(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position37537842
GeneSNIP1
is asnp
is mentioned by
dbSNPrs387906986
ebirs387906986
HLIrs387906986
Exacrs387906986
Varsomers387906986
Maprs387906986
PheGenIrs387906986
hapmaprs387906986
1000 genomesrs387906986
hgdprs387906986
ensemblrs387906986
gopubmedrs387906986
geneviewrs387906986
scholarrs387906986
googlers387906986
pharmgkbrs387906986
gwascentralrs387906986
openSNPrs387906986
23andMers387906986
23andMe allrs387906986
SNP Nexus

SNPshotrs387906986
SNPdbers387906986
MSV3drs387906986
GWAS Ctlgrs387906986
Max Magnitude0
ClinVar
Risk rs387906986(G;G)
Alt rs387906986(G;G)
Reference rs387906986(A;A)
Significance Pathogenic
Disease Psychomotor retardation
Variation info
Gene SNIP1
CLNDBN Psychomotor retardation, epilepsy, and craniofacial dysmorphism
Reversed 1
HGVS NC_000001.10:g.38003443T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023695.2,