Variant (rsID / SNP)

rs35337578

rs35337578 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SKIC2, DXO. Location: chromosome 6, position 31,938,451. Clinical significance in the table: Benign.

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Reference-table entries

SKIC2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:31938451
Cytoband: 6p21.33
HGVS: NM_005510.4(DXO):c.744A>G (p.Pro248_Thr249=)
Allele change: Synonymous_P248P

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.