Rs104893896

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893896(A;A)
Make rs104893896(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position174729294
GeneMSX2
is asnp
is mentioned by
dbSNPrs104893896
Exacrs104893896
PheGenIrs104893896
nextbiors104893896
hapmaprs104893896
1000 genomesrs104893896
hgdprs104893896
ensemblrs104893896
gopubmedrs104893896
geneviewrs104893896
scholarrs104893896
googlers104893896
pharmgkbrs104893896
gwascentralrs104893896
openSNPrs104893896
23andMers104893896
23andMe allrs104893896
SNP Nexus

SNPshotrs104893896
SNPdbers104893896
MSV3drs104893896
Max Magnitude0
OMIM123101
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893896(A;A)
Alt rs104893896(A;A)
Reference rs104893896(G;G)
Significance Pathogenic
Disease Parietal foramina 1
Variation info
Gene MSX2
CLNDBN Parietal foramina 1
Reversed 0
HGVS NC_000005.9:g.174156297G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018476.26,