Variant (rsID / SNP)

rs4447263

rs4447263 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHX37. Location: chromosome 12, position 125,434,580. The table records no clinical significance for this variant.

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Reference-table entries

DHX37Not classified

Variant type: missense_variant
Chromosome / position: 12:125434580
HGVS: NM_032656.4,c.3242G>A,p.Arg1081Gln
Allele change: Missense_R1081Q

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.