Variant (rsID / SNP)

rs17031387

rs17031387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCHS2. Location: chromosome 4, position 155,219,361. The table records no clinical significance for this variant.

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Reference-table entries

DCHS2Not classified

Variant type: synonymous_variant
Chromosome / position: 4:155219361
HGVS: NM_001358235.2,c.6105T>C,p.Asp2035Asp
Allele change: Synonymous_D2035D

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.