Variant (rsID / SNP)

rs902321

rs902321 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SUCLG2. Location: chromosome 3, position 67,411,166. Clinical significance in the table: Benign.

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Reference-table entries

SUCLG2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:67411166
Cytoband: 3p14.1
HGVS: NM_001177599.2(SUCLG2):c.1210T>C (p.Tyr404His)
Allele change: Missense_Y404H

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.