PSG2 pregnancy specific beta-1-glycoprotein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 76 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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88 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CEA |
SYNONYM | PSBG2 |
SYNONYM | PSG1 |
MIM | 176391 OMIM |
HGNC | HGNC:9519 HGNC |
Ensembl | ENSG00000242221 Ensembl |
AllianceGenome | HGNC:9519 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000406487.6 | hg38 | chr19 | 43,064,209 | 43,082,701 | 18,493 |
ENST00000406487.6 | hg19 | chr19 | 43,568,361 | 43,586,853 | 18,493 |
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