Variant (rsID / SNP)
rs1352714
rs1352714 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCHS2. Location: chromosome 4, position 155,243,604. The table records no clinical significance for this variant.
Reference-table entries
DCHS2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:155243604
- HGVS
- NM_001358235.2,c.4055A>G,p.Asn1352Ser
- Allele change
- Missense_N1352S
Associated conditions / phenotypes
Graves' Disease|Hyperthyroidism|Periodic Paralysis|Thyrotoxic Periodic Paralysis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.