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rs1057519205

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519205(A;A)
Make rs1057519205(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position72265053
GeneRIMS1
is asnp
is mentioned by
dbSNPrs1057519205
dbSNP (old)rs1057519205
ClinGenrs1057519205
ebirs1057519205
HLIrs1057519205
Exacrs1057519205
Gnomadrs1057519205
Varsomers1057519205
LitVarrs1057519205
Maprs1057519205
PheGenIrs1057519205
Biobankrs1057519205
1000 genomesrs1057519205
hgdprs1057519205
ensemblrs1057519205
gopubmedrs1057519205
geneviewrs1057519205
scholarrs1057519205
googlers1057519205
pharmgkbrs1057519205
gwascentralrs1057519205
openSNPrs1057519205
23andMers1057519205
23andMe allrs1057519205
SNPshotrs1057519205
SNPdbers1057519205
MSV3drs1057519205
GWAS Ctlgrs1057519205
Max Magnitude0
ClinVar
Risk rs1057519205(A;A)
Alt rs1057519205(A;A)
Reference Rs1057519205(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RIMS1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.72974756G>A
CLNSRC
CLNACC RCV000415728.1,