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DSCAML1 c.512-118730A>G
Variant ID: 11-117521967-T-C
NM_020693.4(
DSCAML1
):c.512-118730A>G
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Allelic variation in gene expression is common in the human genome.
Genome Research
Lo, H Shuen HS; Wang, Zhining Z; Hu, Ying Y; Yang, Howard H HH; Gere, Sheryl S; Buetow, Kenneth H KH; Lee, Maxwell P MP
Publication Date: 2003-08
Variant appearance in text: rs16867
PubMed Link:
12902379
Variant Present in the following documents:
Main text
View BVdb publication page