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rs1057520695

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520695(C;G)
Make rs1057520695(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position183092514
GeneMCCC1
is asnp
is mentioned by
dbSNPrs1057520695
dbSNP (old)rs1057520695
ClinGenrs1057520695
ebirs1057520695
HLIrs1057520695
Exacrs1057520695
Gnomadrs1057520695
Varsomers1057520695
Maprs1057520695
PheGenIrs1057520695
Biobankrs1057520695
1000 genomesrs1057520695
hgdprs1057520695
ensemblrs1057520695
gopubmedrs1057520695
geneviewrs1057520695
scholarrs1057520695
googlers1057520695
pharmgkbrs1057520695
gwascentralrs1057520695
openSNPrs1057520695
23andMers1057520695
23andMe allrs1057520695
SNPshotrs1057520695
SNPdbers1057520695
MSV3drs1057520695
GWAS Ctlgrs1057520695
Max Magnitude0
ClinVar
Risk rs1057520695(G;G)
Alt rs1057520695(G;G)
Reference Rs1057520695(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.182810302G>C
CLNSRC
CLNACC RCV000441741.1,