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rs606231464

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231464(-;-)
Make rs606231464(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110183003
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs606231464
ebirs606231464
HLIrs606231464
Exacrs606231464
Varsomers606231464
Maprs606231464
PheGenIrs606231464
hapmaprs606231464
1000 genomesrs606231464
hgdprs606231464
ensemblrs606231464
gopubmedrs606231464
geneviewrs606231464
scholarrs606231464
googlers606231464
pharmgkbrs606231464
gwascentralrs606231464
openSNPrs606231464
23andMers606231464
23andMe allrs606231464
SNP Nexus

SNPshotrs606231464
SNPdbers606231464
MSV3drs606231464
GWAS Ctlgrs606231464
Max Magnitude0
ClinVar
Risk rs606231464(;)
Alt rs606231464(;)
Reference rs606231464(C;C)
Significance Pathogenic
Disease Brain small vessel disease with hemorrhage
Variation info
Gene COL4A1
CLNDBN Brain small vessel disease with hemorrhage
Reversed 1
HGVS NC_000013.10:g.110835350delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000148943.5,