Variant (rsID / SNP)

rs360042

rs360042 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNC. Location: chromosome 1, position 33,160,878. The table records no clinical significance for this variant.

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Reference-table entries

SYNCNot classified

Variant type: missense_variant
Chromosome / position: 1:33160878
HGVS: NM_030786.3,c.821G>A,p.Arg274Gln
Allele change: Missense_R274Q

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.