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rs1057520543

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520543(G;G)
Make rs1057520543(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position43650480
GeneRSPH9
is asnp
is mentioned by
dbSNPrs1057520543
dbSNP (old)rs1057520543
ClinGenrs1057520543
ebirs1057520543
HLIrs1057520543
Exacrs1057520543
Gnomadrs1057520543
Varsomers1057520543
Maprs1057520543
PheGenIrs1057520543
Biobankrs1057520543
1000 genomesrs1057520543
hgdprs1057520543
ensemblrs1057520543
gopubmedrs1057520543
geneviewrs1057520543
scholarrs1057520543
googlers1057520543
pharmgkbrs1057520543
gwascentralrs1057520543
openSNPrs1057520543
23andMers1057520543
23andMe allrs1057520543
SNPshotrs1057520543
SNPdbers1057520543
MSV3drs1057520543
GWAS Ctlgrs1057520543
Max Magnitude0
ClinVar
Risk rs1057520543(G;G)
Alt rs1057520543(G;G)
Reference Rs1057520543(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RSPH9
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.43618217T>G
CLNSRC
CLNACC RCV000431583.1,