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rs398122877

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122877(-;-)
Make rs398122877(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position64192020
GeneAMER1
is asnp
is mentioned by
dbSNPrs398122877
ebirs398122877
HLIrs398122877
Exacrs398122877
Varsomers398122877
Maprs398122877
PheGenIrs398122877
hapmaprs398122877
1000 genomesrs398122877
hgdprs398122877
ensemblrs398122877
gopubmedrs398122877
geneviewrs398122877
scholarrs398122877
googlers398122877
pharmgkbrs398122877
gwascentralrs398122877
openSNPrs398122877
23andMers398122877
23andMe allrs398122877
SNP Nexus

SNPshotrs398122877
SNPdbers398122877
MSV3drs398122877
GWAS Ctlgrs398122877
Max Magnitude0
ClinVar
Risk rs398122877(;)
Alt rs398122877(;)
Reference rs398122877(C;C)
Significance Pathogenic
Disease Osteopathia striata with cranial sclerosis
Variation info
Gene AMER1
CLNDBN Osteopathia striata with cranial sclerosis
Reversed 1
HGVS NC_000023.10:g.63411900delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000030705.7,