Variant (rsID / SNP)

rs6601444

rs6601444 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSRA. Location: chromosome 8, position 10,211,175. The table records no clinical significance for this variant.

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Reference-table entries

MSRANot classified

Variant type: intron_variant
Chromosome / position: 8:10211175
HGVS: NM_012331.5,c.543+33676C>T
Allele change: Silent

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.