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rs201855602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201855602(A;A)
Make rs201855602(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position94043470
GeneABCA4
is asnp
is mentioned by
dbSNPrs201855602
dbSNP (classic)rs201855602
ClinGenrs201855602
ebirs201855602
HLIrs201855602
Exacrs201855602
Gnomadrs201855602
Varsomers201855602
LitVarrs201855602
Maprs201855602
PheGenIrs201855602
Biobankrs201855602
1000 genomesrs201855602
hgdprs201855602
ensemblrs201855602
geneviewrs201855602
scholarrs201855602
googlers201855602
pharmgkbrs201855602
gwascentralrs201855602
openSNPrs201855602
23andMers201855602
SNPshotrs201855602
SNPdbers201855602
MSV3drs201855602
GWAS Ctlgrs201855602
Max Magnitude0
ClinVar
Risk rs201855602(A;A)
Alt rs201855602(A;A)
Reference Rs201855602(G;G)
Significance Pathogenic
Disease Stargardt disease 1 not provided
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1 not provided
Reversed 0
HGVS NC_000001.10:g.94509026G>A
CLNSRC
CLNACC RCV000406318.1, RCV000412846.1,