Variant (rsID / SNP)

rs10017772

rs10017772 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCHS2. Location: chromosome 4, position 155,287,535. The table records no clinical significance for this variant.

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Reference-table entries

DCHS2Not classified

Variant type: missense_variant
Chromosome / position: 4:155287535
HGVS: NM_001358235.2,c.2303A>G,p.His768Arg
Allele change: Missense_H768R

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.