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rs869320663

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320663(-;-)
Make rs869320663(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position19975756
GeneRIN2
is asnp
is mentioned by
dbSNPrs869320663
ebirs869320663
HLIrs869320663
Exacrs869320663
Varsomers869320663
Maprs869320663
PheGenIrs869320663
hapmaprs869320663
1000 genomesrs869320663
hgdprs869320663
ensemblrs869320663
gopubmedrs869320663
geneviewrs869320663
scholarrs869320663
googlers869320663
pharmgkbrs869320663
gwascentralrs869320663
openSNPrs869320663
23andMers869320663
23andMe allrs869320663
SNP Nexus

SNPshotrs869320663
SNPdbers869320663
MSV3drs869320663
GWAS Ctlgrs869320663
Max Magnitude0
ClinVar
Risk rs869320663(;)
Alt rs869320663(;)
Reference rs869320663(C;C)
Significance Pathogenic
Disease Macrocephaly
Variation info
Gene RIN2
CLNDBN Macrocephaly, alopecia, cutis laxa, and scoliosis
Reversed 0
HGVS NC_000020.10:g.19956400delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001359.4,