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rs104893853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893853(A;A)
Make rs104893853(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position4862854
GeneMSX1
is asnp
is mentioned by
dbSNPrs104893853
ebirs104893853
HLIrs104893853
Exacrs104893853
Varsomers104893853
Maprs104893853
PheGenIrs104893853
hapmaprs104893853
1000 genomesrs104893853
hgdprs104893853
ensemblrs104893853
gopubmedrs104893853
geneviewrs104893853
scholarrs104893853
googlers104893853
pharmgkbrs104893853
gwascentralrs104893853
openSNPrs104893853
23andMers104893853
23andMe allrs104893853
SNP Nexus

SNPshotrs104893853
SNPdbers104893853
MSV3drs104893853
GWAS Ctlgrs104893853
Max Magnitude0
OMIM142983
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893853(A,G;A,G)
Alt rs104893853(A,G;A,G)
Reference rs104893853(C;C)
Significance Pathogenic
Disease Hypoplastic enamel-onycholysis-hypohidrosis syndrome
Variation info
Gene MSX1
CLNDBN Hypoplastic enamel-onycholysis-hypohidrosis syndrome
Reversed 0
HGVS NC_000004.11:g.4864581C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016011.25,