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rs606231371

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs606231371(-;-)
Make rs606231371(-;TCCT)
Make rs606231371(TCCT;TCCT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position108681851
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs606231371
ebirs606231371
HLIrs606231371
Exacrs606231371
Varsomers606231371
Maprs606231371
PheGenIrs606231371
hapmaprs606231371
1000 genomesrs606231371
hgdprs606231371
ensemblrs606231371
gopubmedrs606231371
geneviewrs606231371
scholarrs606231371
googlers606231371
pharmgkbrs606231371
gwascentralrs606231371
openSNPrs606231371
23andMers606231371
23andMe allrs606231371
SNP Nexus

SNPshotrs606231371
SNPdbers606231371
MSV3drs606231371
GWAS Ctlgrs606231371
Max Magnitude0
ClinVar
Risk rs606231371(TCCT;TCCT)
Alt rs606231371(TCCT;TCCT)
Reference rs606231371(;)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107925081_107925082insTCCT
CLNSRC
CLNACC RCV000021587.1,