Variant (rsID / SNP)

rs1044303

rs1044303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMLR1, EPB41L2. Location: chromosome 6, position 131,148,737. The table records no clinical significance for this variant.

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Reference-table entries

SMLR1Not classified

Variant type: missense_variant
Chromosome / position: 6:131148737
HGVS: NM_001195597.2,c.184G>A,p.Val62Met
Allele change: Missense_V62M

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.