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rs878854998

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854998(-;-)
Make rs878854998(-;A)
Make rs878854998(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position73449543
GeneALMS1
is asnp
is mentioned by
dbSNPrs878854998
ebirs878854998
HLIrs878854998
Exacrs878854998
Varsomers878854998
Maprs878854998
PheGenIrs878854998
hapmaprs878854998
1000 genomesrs878854998
hgdprs878854998
ensemblrs878854998
gopubmedrs878854998
geneviewrs878854998
scholarrs878854998
googlers878854998
pharmgkbrs878854998
gwascentralrs878854998
openSNPrs878854998
23andMers878854998
23andMe allrs878854998
SNP Nexus

SNPshotrs878854998
SNPdbers878854998
MSV3drs878854998
GWAS Ctlgrs878854998
Max Magnitude0
ClinVar
Risk rs878854998(A;A)
Alt rs878854998(A;A)
Reference rs878854998(;)
Significance Pathogenic
Disease Alstrom syndrome
Variation info
Gene ALMS1
CLNDBN Alstrom syndrome
Reversed 0
HGVS NC_000002.11:g.73676670dupA
CLNSRC
CLNACC RCV000229272.1,